Specialisms
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Biometrics
We connect SAS programmers, data managers and data scientists with the latest opportunities within CROs and pharmaceutical companies.
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Commercial
Versed in the ever-changing commercial landscape, our team place professionals across a variety of verticals including marketing, sales, HEOR, market access and legal.
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Clinical Operations
In support of some of the most innovative pharmaceutical and biotechnology companies and leading CROs, our team source professionals for stages I - IV clinical trials across Europe and the US.
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Medical
We work with industry leaders in biopharmaceuticals, medical devices and CROs and support their growth in the medical affairs and clinical development space.
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RA, QA and Validation
An essential part of the drug development cycle, our dedicated team work with clients in the quality assurance, quality control, regulatory and validation fields across Europe and further afield.
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Research and Development
Those we work with rely on us to pair top talent with boundary-pushing R&D departments to ensure they can continue supporting the patient population through research activities.
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Technical Operations
From manufacturing to product development, facilities management to engineering, our team understand the skills necessary to ensure the success of a tech ops department.
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Support and Administration
Our partners trust us when it comes to connecting professionals with opportunities across all aspects of their business, including support and administrative roles.
Find your next role.
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Senior Director Biometry - Biotech
Paris |
Negotiable
Senior Director BiometricsLocation: Paris, FRANCEIn this role, the Senior Director will be responsible for driving the company's Biometrics activities for all studies including supervision of biostatistics, programming, and Data Management activities.Job Responsibilities include (but are not limited to):- Defining and delivering the vision and goals for the Biometrics department- Ensuring statistical leadership within the Biometrics department.- Leading statistical strategy as well as clinical development plans and regulatory submissions.- Supporting the clinical study team on the collection, interpretation and reporting of clinical data.- Providing support / coordinate statistical methodology and technical guidance.- Managing department resource allocation to support all clinical trial projects.- Supervising the Biometrics team which includes recruitment if needed, team members development, target setting, performance management and mentoring.- Networking with partners, Building and maintaining effective strategic working relationships such as industry, academic, professional and other organizations.- Responsible for GCP compliance and Standard Operating Procedures (SOPs).- Serve as a statistical consultant for other members of the department and staff members from other departments within the company.Required Skills and Qualification:- PhD in biostatistics or related field and at least 12 years relevant experience.- Master's degree in biostatistics or related field and at least 15 years relevant experience.- 15 years' experience in biostatistics within the Pharma/Biotech/CRO industry.- Project Management Required.- International experience preferred.Technical capabilities:- At least 15 years' experience in clinical drug development & Statistical expertise with emphasis in late clinical stage.- Strong experience of regulatory interactions and submissions in Europe and US- Strong interest in driving innovation and capabilities in supervising scientific/technical work.- In depth knowledge of applicable clinical research regulatory requirements and international statistical guidelines (i.e. ICH GCP).- Strong skills in developing people and teams.- Excellent communication skills
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(Senior) Clinical Research Associate
France |
€47000 - €57000 per annum
I am currently seeking an individual to join a small CRO in a permanent, home based position as a Clinical Research Associate II / Senior Clinical Research Associate. The CompanyThe company itself are a small CRO with a strong oncology pipeline. They have a number of exciting studies that you will be working on a from start-up through to close-out and, as the company is smaller in size, this means that you will have much broader scope of responsibilities at site level (e.g. overseeing site budgets and start-up activities) and more visibility and scale to grow within the role. The company also adopt a quality over quantity approach when it comes to monitoring and they truly value and reward those going above and beyond in their duties with great career progression opportunities. The RoleMain responsibilities include, but are not limited to;* Completing site selection, pre-study start up activities and assisting in site evaluation* Managing investigative site activity to ensure satisfactory study understanding and compliance of all site staff and providing updates to the Study Manager as necessary.* Oversee study start-up or site management activities such as helping with regulatory submissions to Ethic Committees, contract negotiation and budget negotiation.* Completion of monitoring reports and follow-up letters; including all key findings and recommendations for future actions.* Maintaining Trial Master File (TMF)/electronic Trial Master File (eTMF).* May provide training, mentoring, and co-monitoring alongside junior CRA's as required. The PersonRequirements are as follows;* Minimum 2 years independent, on-site monitoring experience.* BSc in a Life Science related discipline (higher degrees very desirable).* Experience as CRA/Clinical Monitor in CRO/Pharma/Biotech essential.* Experience within oncology essential. * Professional proficiency in both English and French.This is a fantastic opportunity for anyone looking to join a close-knit company who adopt a quality over quantity approach and who truly value to work of their employees. So, if you feel that you would be a good fit or you simply want to find out more about this role, then don't delay and apply today!If this isn't the role for you but you know someone that would be suitable, tell them to drop me an email or give me a call, my contact details are below. E: rebecca.law@SECpharma.comT: +44 (0)2072556600
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(Senior) Clinical Research Associate - Sponsor Dedicated
Romenay |
€48000.00 - €58000.00 per annum
I am currently seeking an individual to join a reputable CRO in a permanent, home based position as a sponsor dedicated Clinical Research Associate II / Senior Clinical Research Associate. The CompanyYou will be working outsourced to a leading pharmaceutical company who have an extensive pipeline within Oncology, across both early and late stage development, as well as additional therapy areas such as Neurology and Infectious Diseases. You will be tasked with carrying out a mix of remote and on-site monitoring visits (largely remote due to the current climate) with scope to take on additional responsibilities, such as training and co-monitoring alongside junior CRA's, as your seniority level within the clinical monitoring team grows.The RoleMain responsibilities include, but are not limited to;* Completing site selection, pre-study start up activities and assisting in site evaluation* Managing investigative site activity to ensure satisfactory study understanding and compliance of all site staff and providing updates to the Study Manager as necessary.* Oversee study start-up or site management activities such as helping with regulatory submissions to Ethic Committees, contract negotiation and budget negotiation.* Completion of monitoring reports and follow-up letters; including all key findings and recommendations for future actions.* Maintaining Trial Master File (TMF)/electronic Trial Master File (eTMF).* May provide training, mentoring, and co-monitoring alongside junior CRA's as required. The PersonRequirements are as follows;* Minimum 2 years independent, on-site monitoring experience.* BSc in a Life Science related discipline (higher degrees very desirable).* CRA Certification according to Ministerial Decree dated 15/11/2011.* Experience as CRA/Clinical Monitor in CRO/Pharma/Biotech essential.* Experience within oncology essential. * Professional proficiency in both English and Italian.This is a fantastic opportunity for anyone who is interested in working within the sponsor side of clinical trials whilst having the support of a reputable CRO who can offer competitive packages and development opportunities, to ensure you continue to grow within your career as a CRA. So, if you feel that you would be a good fit or you simply want to find out more about this role, then don't delay and apply today!If this isn't the role for you but you know someone that would be suitable, tell them to drop me an email or give me a call, my contact details are below. E: rebecca.law@SECpharma.comT: +44 (0)2072556620
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Medical Affairs Statistician (Associate Director) - [Germany]
Germany |
€80000 - €100000 per annum
- Oversee and contribute to HTA activities from a statistical perspective;- Develop statistical related documents, including statistical reports;- Participate and contribute to the department's strategy development.An exciting opportunity has become available as Associate Director, Statistics with a global Biopharma to be based in Germany on permanent basis. The company is recognized for its warm, open minded working culture and development opportunities, as such they secured a top place in the industry.In this role you will actively contribute to statistical strategy on project level and work close with key departments such as Clinical, HEOR and Programming one. Your exposure will be focusing on medical affairs statistics with exposure also to clinical development, and be involved/oversee submissions with local authorities. The successful candidate will have:- MSc (or above) in Medical Statistics, Applied Mathematics, Life Sciences or related analytical fields; - Demonstrable experience with meta-analysis;- Solid experience in project leading from a statistical perspective;- Strong experience in HEOR / HTA / RWE;- Extended SAS OR R programming experience;- Excellent communication skills and ability to adapt to different audiences.If you are interested in learning more about this great opportunity, do not hesitate to get in touch at catalin.zaharia@secpharma.com or +44 (0)20 7255 6610Catalin ZahariaPrincipal Consultant - Life SciencesBiometrics - SAS Programming, Biostatistics, Data Management, Data AnalyticsTel: +44 (0) 207 255 66 65Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia
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Associate Director, Statistical Programming [Homebased]
England |
£75000 - £90000 per annum + Bonus & Standard Benefits
Statistical Programming, Associate DirectorUK & Europe - home basedCompetitive package A scientific focused CRO is looking to appoint an Associate Director, Statistical Programming and work close with cross functions departments such as Biostatistics, Data Management and lead the biometrics operations within the business. This opportunity will be serving a technical experienced individual that would like to develop a strong and stable career in global business working close with an European based team.As Associate Director, Statistical Programming you will lead biometrics operations with related departments - Biostatistics, Statistical Programming, Data Management - and manage projects in clinical trials (from Phase I to submission). You will also functionally lead a team of experienced programmers and if needed will contribute with hands on tasks to meet the commitments.You will communicate with stakeholders the results, strategy and actively participate in developing tools and operational prototypes that will support the vision and strategy of the business.The successful candidate will have:* MSc in Computer Programming or Life Sciences - PhD would be preferred;* Minimum of 8 years of SAS Programming experience developed in Pharma/Biotech/CRO;* Strong clinical trials experience, ideally from phase I - III;* Extensive knowledge of CDISC standards and industry's regulation; * Strong communication skills with ability to adapt to different audiences;* SAS Certifications would be desired;* A structured mindset that will be reflected in work and communication.This is a fantastic opportunity to join a scientific focused CRO with great market longevity which has contributed to top selling products in the market in key therapeutic areas.If you looking to learn more about this Associate Director SAS Programming role with one of the most reputable and respected names in the industry, do not hesitate to get in touch for a confidential chat, alternatively send your CV to:Catalin ZahariaPrincipal Consultant - Life Sciences Biometrics - SAS Programming, Biostatistics, Data Management, Data AnalyticsTel: +44 (0) 207 255 66 65Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia
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SAP Consultants
Milano, Milan (province) |
Up to £0.00 per annum
Consulenti SAP:SAP FI, SAP FM, SAP MM, SAP SD, SAP PP, SAP SD LE-TRA, SAP PM, SAP WM/EWM, SAP SUCCESSFACTORS*posizioni multiple per consulenti di diverse Seniority (Analyst / Consultant / Senior Consultant / Manager). Location: Milano, Roma, Torino Tipologia: contratto a tempo indeterminato Inizio: ASAP Una delle più importanti e dinamiche aziende di System Integration ricerca consulenti SAP per diverse sedi in Italia. In seguito ad una forte crescita del business, in continua evoluzione, l'azienda cerca consulenti SAP con diversi livelli di esperienza nelle attività di analisi funzionale, customizing, implementazione e gestione di soluzioni applicative. La Societa' offre interessanti percorsi di carriera, rendendo disponibile un'ampia varietà di ruoli, a partire dal Business Analyst fino alle posizioni manageriali. In particolare siamo interessati ad entrare in contatto con consulenti in possesso di determinate caratteristiche:Minimo 2 anni di esperienzaEsperienza di almeno 2 full implementation life cyclesBuona padronanza della lingua inglese, scritta e parlataDisponibilita' a trasferte Per le posizioni di livello manageriale cerchiamo candidati che abbiano anche esperienza pregressa di:Team managementPre salesGestione di budget di progetto Completano il profilo:Forte attitudine e propensione al team workingProblem solving Cerchiamo candidati dalla mente aperta, che siano in grado di proporre soluzioni innovative per i Clienti Finali, persone capaci di fare la differenza.Ti riconosci in questa descrizione?Potrai fare parte di un vivace network globale e di un team di persone impegnate in un continuo ampliamento delle proprie skills, offrendo ai Clienti Finali soluzioni di alto livello.Possiamo aprirti possibilità di carriera coinvolgendoti nella realizzazione di progetti importanti e all'avanguardia, grazie alla presenza globale dell'azienda, alle forti e longeve relazioni con i Clienti e grazie a una partnership strategica con il Vendor che da 40 anni consente di ideare e implementare le più innovative soluzioni di business. Queste sono posizioni a tempo indeterminato che offrono un'eccellente opportunità di partecipare come parte attiva ai diversi progetti.Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca Letizia.
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Servicenow Consultant (developer / analyst / manager)
Milano, Milan (province) |
Negotiable
ServiceNow Consultant (developer / analyst / manager)Location: Milano - RomaTipologia: contratto a tempo indeterminato Inizio: ASAPUna delle più importanti e dinamiche aziende multinazionali di System Integration ricerca Consulenti Servicenow per le sue sedi di Milano e Roma.Avrai l'opportunità di operare all'interno di progetti prestigiosi e di alto valore tecnologico, in veste di sviluppatore, analista o consulente, fino alle figure manageriali, a seconda dell'esperienza maturata.Siamo interessati ad entrare in contatto anche con candidati che abbiano competenze di sviluppo (es AngularJS) e che siano interessati ad acquisire competenze e a crescere velocemente su una tecnologia in forte espansione come Servicenow.I requisiti:*Esperienza nell'implementazione e gestione di piattaforme di service management (ServiceNow, Bmc Remedy)*Minimo 6 mesi di esperienza nell'utilizzo di Javascript, Jquery, HTML o AngularJS*Competenze base in ITIL v3, SQLPer le posizioni di livello manageriale cerchiamo candidati che abbiano anche esperienza pregressa di:* Team management* Pre sales* Gestione di budget di progettoCerchiamo candidati dalla mente aperta, dinamici e proattivi, persone capaci di fare la differenza. Ti riconosci in questa descrizione?Potrai fare parte di un vivace network globale e di un team di persone impegnate in un continuo ampliamento delle proprie skills, offrendo ai Clienti Finali soluzioni di alto livello. Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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Programming Manager - [Germany]
Germany |
Negotiable
One of my clients, a top 10 global pharma, is looking to expand the programming team with a Manager, Statistical SAS Programmer in Germany - role can be home based based on the level of experience. This is an exciting time to join the company since they are looking to internalize programming activities, therefore there is expected to have a stable and constant development in the following year. As Statistical Programming Manager you will lead biometrics operations with related departments - Biostatistics, Statistical Programming, Data Management - and manage projects in phase I to III clinical trials. You will also functionally lead a team of experienced programmers and, with the support and training provided, you will be expected to step into a line management role for a small team of programmers.You will also lead internal initiatives, communicate with stakeholders the results, strategy and actively participate in developing tools and operational prototypes that will support the vision and strategy of the department.The successful candidate will have:*MSc in Computer Programming or Life Sciences;*Minimum of 8 years of SAS Programming experience developed in Pharma/Biotech/CRO;*Strong clinical trials experience, ideally in phase II and III trials;*Excellent knowledge of CDISC standards with emphasis on ADaM and TFLs; *Strong communication skills with ability to adapt to different audiences;*People management experience would be a massive advantage;*A structured mindset that will be reflected in work and communication.If you looking to learn more about this great Statistical Programming Manager role with one of the most reputable and respected names in the industry, do not hesitate to get in touch for a confidential and friendly chat, alternatively send your CV to:Catalin ZahariaPrincipal Consultant - Life Sciences RecruitmentBiometrics - SAS Programming, Biostatistics, Data ManagementTel: +44 (0) 207 255 66 10Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia
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Statistical Programming Manager - Switzerland
Switzerland |
My client, a scientific focused Biopharma, is looking to appoint a Statistical Programming Manager and work close with cross functions departments such as Biostatistics, Data Management and lead the biometrics operations within the business. This opportunity will be serving a technical experienced individual that would like to develop a strong and stable career in global business working close with a team from European locations and actively contribute to development and updating processes aligned with the programming activities.As Statistical Programming Manager you will lead biometrics operations with related departments - Biostatistics, Statistical Programming, Data Management - and manage projects in phase I to III clinical trials. You will also functionally lead a team of experienced programmers and, with the support and training provided, you will be expected to step into a line management role for a small team of programmers.You will also lead internal initiatives, communicate with stakeholders the results, strategy and actively participate in developing tools and operational prototypes that will support the vision and strategy of the department.The successful candidate will have:*MSc in Computer Programming or Life Sciences;*Minimum of 8 years of SAS Programming experience developed in Pharma/Biotech/CRO;*Strong clinical trials experience, ideally in phase II and III trials;*Excellent knowledge of CDISC standards with emphasis on ADaM and TFLs; *Strong communication skills with ability to adapt to different audiences;*People management experience would be a massive advantage;*A structured mindset that will be reflected in work and communication.This is a fantastic opportunity to join a scientific focused Pharma with a solid pipeline of products in development. You will be welcomed in a supportive working culture where you will benefit from a mixed exposure and superb career opportunities to meet your objectives.If you looking to learn more about this Statistical Programming Manager role, do not hesitate to get in touch for a confidential chat, alternatively send your CV to:Catalin ZahariaPrincipal Consultant - Life Sciences RecruitmentBiometrics - SAS Programming, Biostatistics, Data ManagementTel: +44 (0) 207 255 66 10Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia#SAS #CDISC #SDTM #ADaM #MACRO #clinicaltrials #biopharma #CRO
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Senior Data Manager - Switzerland
Switzerland |
A global leader within pharmaceutical industry is looking for a experienced Data Managers to join the growing team. This is a fantastic opportunity to advance your career to the next level and take leadership on study level from a DM perspective. You will be provided with superb training and development opportunities that will support your growth.As Lead Data Manager you will be responsible of all Data Management activities on project level, essentially you will take leadership on study level and ensure quality deliverables on time and within budget. You will act as SME - subject matter expert - and provide leadership and vision to the team, drive process standardisation and manage vendors.The successful candidate will have:- BSc in life sciences with 3 years of DM experience within pharma sector; - Proven leadership experience on study level - acting as Project Lead from a DM perspective;- Excellent communication skills - able to manage clients;- Ability to work in a multicultural environment;- Proactive, team-oriented attitude;- Other programming languages knowledge like S-Plus, R, etc would be an advantage;If you're looking to work with a leading global organization that will provide excellent development options, this is the right opportunity for you! You will work close with some of the brightest individuals in life-changing projects helping and transforming the millions of patients out there. Don't hesitate and get in touch for a confidential chat about this Lead Data Manager role and please send your updated CV to:Catalin ZahariaSenior Consultant - BiometricsTel: +44 (0) 207 255 66 10Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia
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Statistical Programming Manager
England |
€65000 - €80000 per annum + Bonus & Standard Benefits
Statistical Programming Manager - Europe (home based)Team based in Europe A new exciting opportunity is available for an experienced SAS Programmer to joining a world recognised CRO home based from EU or UK. The company has contributed to the developed of key products in demanded therapeutic areas and their consultative and quality focused approach puts them apart from their competitors. My client has secured one of the lowest staff turn-over rate industry through the working culture and development opportunities. This is a place where you can grow and develop further your programming skills, while benefiting from a healthy work-life balance. As Programming Manager you will cover a fine mix of activities: line managing a small team of programmers across Europe, while leading complex programming activities on project level - clinical trials. Furthermore you can participate in strategic team initiatives and have a voice in regards to the programming strategy on client/portfolio level. The successful candidate will have: - MSc in Statistics, Applied Mathematics, Life Sciences, or related field; - Over 8 years of programming experience in clinical trials;- Strong leadership experience from a programming perspective; - People management experience;- Solid CDISC experience;- Excellent communication skills and ability to adapt to different audiences;This suits excellent a person which would like to add value from a line management perspective, while keeping a particular touch with the technical side - SAS Programming - in clinical trials.Do not hesitate and get in touch for a confidential chat about this Programming Manager role, alternatively send your CV to:Catalin ZahariaPrincipal Consultant - BiometricsSAS Programming, Biostatistics, Clinical Data ManagementTel: +44 (0) 207 255 66 61Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia#SAS #CDISC #peoplemanagement #CRO #Biopharma #FSP #StatisticalProgramming
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Dir, Translational Medicine
Spain |
Up to €0.00 per annum
A highly innovative Biopharma company focused on the development & commercialisation of cutting-edge treatments for solid and blood cancers is currently looking to hire a physician to join their Clinical Development unit.The company offers a location flexibility, although a relocation to Spain will be needed.You will design and implement early stage clinical studies, collaborate with other company functions such as Translational Development Scientists, Discovery and Development Teams for defining Clinical PD or Biomarker assays.We would like to speak with pharmaceutical industry physicians with extensive clinical development experience in relevant fields and willing to travel when safe and according to business needs.The company offers a very competitive remuneration, a successful and collaborative team of professionals, and the chance to contribute to the development of innovative therapies within Hematology and Oncology.
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Clinical Scientist
Germany |
Up to €0.00 per annum
A global Biotechnology company is looking for Clinical Scientists to join their teams based in Germany.Key tasks will be to implement, plan, and execute assigned clinical trial activities:* Evaluate innovative trial designs in collaboration with Medical Monitor and Clinical Development Lead.* Protocol and ICF development process including writing, reviewing, adjudication/resolution of cross functional comments and ensuring high clinical quality (collaboration with Medical Writing)* data generation and validation, including CRF design, clinical data review/query resolution; ensure quality data review by supporting CS team* support Study Committee activitiesWe are looking for a PhD coupled with 5 years of experience in Clinical Science within Hematology and/or Oncology. Flexibility to travel required.
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Senior Medical Director
England |
Up to Swiss Franc0.00 per annum + Flexible Depending on Experience
(Senior) Medical Director, Clinical Development A highly innovative Gene Therapy Biotechnology company focused on the development & commercialisation of cutting-edge treatments for rare neurological disorders is currently looking to hire a physician to join their multinational Clinical Development unit in the capacity of Senior Medical Director. This new vacancy represents a fantastic opportunity to join an exceptional team with a wealth of experience, developing gene therapies which make a huge impact on the patients and families that have been devastated by serious genetic, neurodegenerative, rare disease.Key tasks will be the design, conduct, execution and reporting of clinical studies, in addition to the responsibility to provide support to the EMEA commercial organisation and to interact with regulatory authorities. Some of the key specific responsibilities will include:*Cross-functional collaboration to develop clinical plans and global regulatory submissions.*Partnership with Clinical Operations to ensure efficient clinical study activities.*Clinical data review and support to clinical and regulatory documentation.*Identification, management, and interaction with vendors, collaborators, and KOLs.*Clinical study design, medical monitoring and execution and results analysis.*Professional relationships with academic and community-based study sites, identifying investigators and clinical academic expertise.*Incorporate Health Economics Outcomes Research requirements into protocol design.*May potentially directly line manage up to 3x line reports in the clinical development team.We would like to speak with pharmaceutical industry physicians with extensive clinical development experience in relevant fields, used to working within a matrix, multi-located structure, and willing to travel when safe and according to business needs. Specific experience and skills include we are looking for include but are not limited to:*Medical Degree (MD) with added qualifications in Neurology, Paediatrics, Genetics or CNS background.*A minimum of 3 years' industry experience, though those with strong academic clinical research experience could be considered at a Medical Director level.*Demonstrable knowledge of regulatory procedures internationally, with prior experience in US and/or European regulatory filing.*The ideal candidate would have prior experience with neurological/neuromuscular and/or orphan products.*Additional postdoctoral training or additional qualifications such as PhD, PharmD, certificate in Pharmaceutical Medicine would be preferred but not a mandatory requirement.The company offers a very competitive remuneration, a unified and collaborative team of professionals, and the chance to play as a lead contributor to the development of gene therapies with the potential to positively impact the lives of patients and their families.
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Senior Medical Director
Spain |
Up to Swiss Franc0.00 per annum + Flexible Depending on Experience
(Senior) Medical Director, Clinical Development A highly innovative Gene Therapy Biotechnology company focused on the development & commercialisation of cutting-edge treatments for rare neurological disorders is currently looking to hire a physician to join their multinational Clinical Development unit in the capacity of Senior Medical Director. This new vacancy represents a fantastic opportunity to join an exceptional team with a wealth of experience, developing gene therapies which make a huge impact on the patients and families that have been devastated by serious genetic, neurodegenerative, rare disease.Key tasks will be the design, conduct, execution and reporting of clinical studies, in addition to the responsibility to provide support to the EMEA commercial organisation and to interact with regulatory authorities. Some of the key specific responsibilities will include:*Cross-functional collaboration to develop clinical plans and global regulatory submissions.*Partnership with Clinical Operations to ensure efficient clinical study activities.*Clinical data review and support to clinical and regulatory documentation.*Identification, management, and interaction with vendors, collaborators, and KOLs.*Clinical study design, medical monitoring and execution and results analysis.*Professional relationships with academic and community-based study sites, identifying investigators and clinical academic expertise.*Incorporate Health Economics Outcomes Research requirements into protocol design.*May potentially directly line manage up to 3x line reports in the clinical development team.We would like to speak with pharmaceutical industry physicians with extensive clinical development experience in relevant fields, used to working within a matrix, multi-located structure, and willing to travel when safe and according to business needs. Specific experience and skills include we are looking for include but are not limited to:*Medical Degree (MD) with added qualifications in Neurology, Paediatrics, Genetics or CNS background.*A minimum of 3 years' industry experience, though those with strong academic clinical research experience could be considered at a Medical Director level.*Demonstrable knowledge of regulatory procedures internationally, with prior experience in US and/or European regulatory filing.*The ideal candidate would have prior experience with neurological/neuromuscular and/or orphan products.*Additional postdoctoral training or additional qualifications such as PhD, PharmD, certificate in Pharmaceutical Medicine would be preferred but not a mandatory requirement.The company offers a very competitive remuneration, a unified and collaborative team of professionals, and the chance to play as a lead contributor to the development of gene therapies with the potential to positively impact the lives of patients and their families.
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Director, Clinical Development - Neurology - Europe Home Based
Belgium |
£100000 - £140000 per annum + Bonus, Benefits, Stock options
(Senior) Medical Director, Clinical Development - NeurologyA highly innovative Biotechnology company focused on the development & commercialisation of cutting-edge treatments for rare neurological disorders is currently looking to hire a physician to join their Clinical Development unit.You will design and implement clinical studies, collaborate with other company functions such as clinical operations, regulatory, biostatistics and drug safety, and will play a key part in producing and interpreting clinical data in addition to document support.We would like to speak with pharmaceutical industry physicians with extensive clinical development experience in relevant fields and willing to travel when safe and according to business needs.The company offers a very competitive remuneration, a successful and collaborative team of professionals, and the chance to contribute to the development of innovative therapies within Neurology.
Apply now -
Senior Medical Director
Switzerland |
Up to Swiss Franc0.00 per annum + Flexible Depending on Experience
(Senior) Medical Director, Clinical DevelopmentSwitzerland or US A highly innovative Gene Therapy Biotechnology company focused on the development & commercialisation of cutting-edge treatments for rare neurological disorders is currently looking to hire a physician to join their multinational Clinical Development unit in the capacity of Senior Medical Director. This new vacancy represents a fantastic opportunity to join an exceptional team with a wealth of experience, developing gene therapies which make a huge impact on the patients and families that have been devastated by serious genetic, neurodegenerative, rare disease.Key tasks will be the design, conduct, execution and reporting of clinical studies, in addition to the responsibility to provide support to the EMEA commercial organisation and to interact with regulatory authorities. Some of the key specific responsibilities will include:*Cross-functional collaboration to develop clinical plans and global regulatory submissions.*Partnership with Clinical Operations to ensure efficient clinical study activities.*Clinical data review and support to clinical and regulatory documentation.*Identification, management, and interaction with vendors, collaborators, and KOLs.*Clinical study design, medical monitoring and execution and results analysis.*Professional relationships with academic and community-based study sites, identifying investigators and clinical academic expertise.*Incorporate Health Economics Outcomes Research requirements into protocol design.*May potentially directly line manage up to 3x line reports in the clinical development team.We would like to speak with pharmaceutical industry physicians with extensive clinical development experience in relevant fields, used to working within a matrix, multi-located structure, and willing to travel when safe and according to business needs. Specific experience and skills include we are looking for include but are not limited to:*Medical Degree (MD) with added qualifications in Neurology, Paediatrics, Genetics or CNS background.*A minimum of 3 years' industry experience, though those with strong academic clinical research experience could be considered at a Medical Director level.*Demonstrable knowledge of regulatory procedures internationally, with prior experience in US and/or European regulatory filing.*The ideal candidate would have prior experience with neurological/neuromuscular and/or orphan products.*Additional postdoctoral training or additional qualifications such as PhD, PharmD, certificate in Pharmaceutical Medicine would be preferred but not a mandatory requirement.The company offers a very competitive remuneration, a unified and collaborative team of professionals, and the chance to play as a lead contributor to the development of gene therapies with the potential to positively impact the lives of patients and their families.
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Medical Science Liaison - Different Locations
Italy |
Negotiable
A global pharmaceutical company is looking for a Medical Science Liaison.You will interact with healthcare organisations and authorities, healthcare professionals, clinical investigators, and other healthcare organisations providing fair, balanced, and scientifically rigorous medical and clinical information.Coordinate advisory boards, build, develop and maintain KOLs and cooperative groups relationships, medical associations and external stakeholders. You may also represent the Medical Department at Local or Regional Medical events (e.g. Medical Congresses and Symposia). We are looking for a life science degree coupled with MSL experience in Italy, and availability for extensive travels.Fluency in Italian and English and deep knowledge of the Italian Health System are mandatory.The successful individual will have demonstrated credibility within the medical community. Will be engaging and able to build strong relationships.EU passport/work permit required.
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Statistical Programming Consultant - 12 months
France |
Negotiable
Contract Statistical Programmer (Europe - home based)Swiss Biopharma 12 months contractI am working exclusively for a Swiss Biopharma which are looking to appoint an experienced Statistical Programmer, home based across Europe.The role will cover the following responsibilities:- Provides functional expertise and leadership to the programming team;- Deliver programming guidance/expertise on clinical projects;- Define/Implement technical solutions and standards for analyzing and reporting clinical data;- Oversee outsourced programming activities. You will have:- MSc in Mathematics, Statistics or related field;- Over 10 years of programming experience in clinical research;- Extensive programming skills, including MACRO standardization;- Solid oversight experience in clinical trials; - Excellent CDISC standards experience, including SDTM, ADaM & TLFs;- Oncology experience/awareness.The role will provide a very generous hourly rate and starting date can be amended based on the candidate's experience. This role is remote based in UK, and in a post-covid context it might require monthly traveling to Switzerland.Do not hesitate and get in touch for a confidential chat about the contract Programming role, alternatively send your CV to:Catalin ZahariaPrincipal Consultant - BiometricsSAS Programming, Biostatistics, Clinical Data ManagementTel: +44 (0) 207 255 66 61Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia#SAS #CDISC #peoplemanagement #CRO #Biopharma #FSP #StatisticalProgramming
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Statistical Programming - Biopharma - All Seniority Levels
England |
£45000 - £70000 per annum + 12%Bonus & standard benefits
A global leading Pharma, well recognized for the working culture and market presence is looking to expand the statistical programming team with multiple Programming roles. They are looking for - Statistical Programmers- Principal Programmers - Technical Manager, ProgrammingThis is a fantastic opportunity to join an organization that promotes an excellent culture and a constant career growth, a place where you will respect your work-life balance and be part of a happy team of experienced programmers on international level.The Programming role will be responsible of taking leadership of the statistical programming activities and create analysis datasets, tables, listing and figures from clinical trial data. You will develop and validate analysis and reporting deliverables on the safety and efficacy side of programming and will collaborate effectively with an international team of programmers.Required Skills and Qualifications:- MSc in Computer Science, Applied Mathematics, Life Sciences or related fields;- Minimum 3 years of statistical programming in clinical trials - ideally in safety and efficacy;- Extended SAS Programming skills, including MACRO, Graphs, and TFLs - tables, figures and listings; - Solid knowledge of the drug development cycle and related guidelines;- Strong analytical mid-set with a particular focus on details;- CDISC experience would be a massive advantage;- Excellent communication skills in English, both verbal and written;If you are looking to join a company with a massive know-how and extended market presence, a business that will invest in your development and will give you the chance to bring innovative ideas and respect your analytical and solution oriented mind-set, look no further! The company has developed innovative products and has a massive pipeline of products that will keep you engaged in your activity. Currently you will be working 100% home based, while in a post-covid context you will be welcomed in their office in London, Munich or Warsaw.Do not hesitate to inquire for more details or to engage in an informal and confidential chat about this Statistical SAS Programming roles with:Catalin ZahariaPrincipal Consultant - Life Sciences RecruitmentBiometrics - SAS Programming, Biostatistics, Clinical Data ManagementTel: +44 (0) 207 255 66 10Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia#sas #CDISC #SDTM #ADaM #clinicalresearch #pharma #statisticalprogramming
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Statistical Programming Consultant - 12 months
England |
Negotiable
Contract Statistical Programmer (UK home based)Swiss Biopharma 12 months contractI am working exclusively for a Swiss Biopharma which are looking to appoint an experienced Statistical Programmer, home based across UK.The role will cover the following responsibilities:- Provides functional expertise and leadership to the programming team;- Deliver programming guidance/expertise on clinical projects;- Define/Implement technical solutions and standards for analyzing and reporting clinical data;- Oversee outsourced programming activities. You will have:- MSc in Mathematics, Statistics or related field;- Over 10 years of programming experience in clinical research;- Extensive programming skills, including MACRO standardization;- Solid oversight experience in clinical trials; - Excellent CDISC standards experience, including SDTM, ADaM & TLFs;- Oncology experience/awareness.The role will provide a very generous hourly rate and starting date can be amended based on the candidate's experience. This role is remote based in UK, and in a post-covid context it might require monthly traveling to Switzerland.Do not hesitate and get in touch for a confidential chat about the contract Programming role, alternatively send your CV to:Catalin ZahariaPrincipal Consultant - BiometricsSAS Programming, Biostatistics, Clinical Data ManagementTel: +44 (0) 207 255 66 61Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia#SAS #CDISC #peoplemanagement #CRO #Biopharma #FSP #StatisticalProgramming
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Lead Biostatistician - 6 months contract
Germany |
Negotiable
Contract Senior/Lead StatisticianDuration: 6 monthsLocations: Europe - home basedSwiss BiopharmaI am recruiting for an innovative Biopharma an exciting opportunity as Senior Statistician, to be home based across Europe and add value to the statistical side of their ongoing trials.Key responsibilities:- support the development plan, statistical design and analysis of clinical studies;- lead the statistical and programming activities on project level;- oversee outsourced activities/CROs;- support the submission process with health authorities.You will have:- MSc in Mathematics, Statistics or related field (PhD desired);- Over 10 years of statistical experience in clinical research;- Extensive SAS programming skills;- Solid oversight experience in clinical trials;- Strong statistical methodology knowledge and implementation (Bayesian is a plus);- Oncology experience/awareness.If you would need further details or if you are interested in applying for this role, pleaseget in touch with Catalin at:Catalin ZahariaPrincipal Consultant - Life SciencesBiometrics - SAS Programming, Biostatistics, Data ManagementTel: +44 (0) 207 255 66 10Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia#Statistics #Biostatistics #SAS #R #clinicalresearch #Biopharma #Pharmaceuticals
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Statistics Manager - Home Based
England |
€70000 - €80000 per annum + Bonus & Standard Benefits
Biostatistics Manager - Europe (home based)Team based in Europe A new exciting opportunity is available for an experienced Statistician to joining a world recognised CRO. The company has contributed to the developed of key products in demanded therapeutic areas and their consultative and quality focused approach puts them apart from their competitors. As Statistics Manager you will actively contribute to biostatistics strategy on project level and have strategic input in relation key clients of the business. Your exposure will be focusing on clinical trials - phase I to III - and will provide leadership and management for a small team of statisticians spread in various European locations. - Lead and line managing a mid-size team of statisticians - Coordinate statistical activities for clinical trials in both, design and reporting - Create project specific strategies and follow up the implementation - Provide leadership and support on individual level for team membersThe successful candidate will have: - MSc in Statistics, Applied Mathematics, Life Sciences, or related field; - Over 8 years of statistical experience in clinical trials;- Strong leadership experience from a statistical perspective in clinical trials; - People management experience;- Experience in applying common methodologies applied to clinical research;- Excellent communication skills and ability to adapt to different audiences;- Knowledge in CDISC standards required;Do not hesitate and get in touch for a confidential chat about this Statistics Manager role, alternatively send your CV to:Catalin ZahariaSenior Consultant - BiometricsSAS Programming, Biostatistics, Clinical Data ManagementTel: +44 (0) 207 255 66 65Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia#Biostatistics #Statistics #CRO #Biopharma #CDISC #statisticalanalysis #clinicalresearch
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Senior Statistical Programmer - Swiss Based
Switzerland |
Swiss Franc120000 - Swiss Franc145000 per annum + Standard Benefits
Catalin Zaharia at SEC Pharma has been retained to source a Senior Statistical Programmer with an innovative Biotech company in Switzerland.The company has a solid pipeline of products in various stages of development, and is looking to secure an autonomous, experienced Programmer to support with programming activities and work close with cross-functional departments such as Biostatistics and Data Management.Those who wish to develop their career in a world class environment - ensuring quality across all programs contact Catalin Zaharia on +44 (0) 207 255 6610 or email Catalin.zaharia@secpharma.comAs Statistical Programmer you will support and oversee clinical trials in phase I to III, and implement & use programs to analyse clinical trials data in a CDISC format. You will review trial documentation and provide your input from a programming point of view. Furthermore you will also have input into procedures and QC-ing practices in place.Your profile:- BSc or above in Scientific discipline;- Over 5 years of SAS programming experience in clinical trials;- Solid CDISC experience, including SDTM and ADaM datasets;- Extended communication skills in EnglishFor a confidential discussion please contact Catalin Zaharia at SEC Pharma on +44 (0) 207 255 6610 or email catalin.zaharia@secpharma.com
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Principal Statistical SAS Programmer - Europe (home based)
England |
£55000 - £68000 per annum + Bonus & standard benefits
A global leader well recognized for the working culture and market presence is looking to expand the statistical programming team with a number of Senior / Principal Statistical SAS Programmers. This is a fantastic opportunity to join an organization that promotes an excellent culture and a constant career growth, a place where you will respect your work-life balance and be part of a happy team of experienced programmers on international level.The Senior or Principal #Statistical #SAS Programmer will be responsible of taking leadership of the statistical programming activities and create analysis datasets, tables, listing and figures from clinical trial data. You will develop and validate analysis and reporting deliverables on the safety and efficacy side of programming and will collaborate effectively with an international team of programmers.Required Skills and Qualifications:- BSc in Computer Science, Applied Mathematics, Life Sciences or related fields;- Minimum 5 years of statistical programming in clinical trials - ideally in safety and efficacy;- Extended SAS Programming skills, including MACRO, Graphs, and TFLs - tables, figures and listings; - Solid knowledge of the drug development cycle and related guidelines;- Strong analytical mid-set with a particular focus on details;- CDISC experience would be a massive advantage;- Excellent communication skills in English, both verbal and written;If you are looking to join a company with a massive know-how and extended market presence, a business that will invest in your development and will give you the chance to bring innovative ideas and respect your analytical and solution oriented mind-set, look no further! Do not hesitate to inquire for more details or to engage confidentially about this Senior / Principal Statistical SAS Programming role with:Catalin ZahariaPrincipal Consultant - Life Sciences RecruitmentBiometrics - SAS Programming, Biostatistics, Data ManagementTel: +44 (0) 207 255 66 10Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia#CDISC #SDTM #ADaM #CRO #Pharma #Biotech #clinicaltrials #biometrics
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Senior Clinical Data Manager - UK & Europe (remote)
England |
€47000 - €58000 per annum + Bonus & Benefits
An exciting opportunity is available for experienced Clinical Data Managers to join a well established CRO on remote basis. The company has developed superb expertise within key therapeutic indications and has secured strategic relationships with specialized Biotech and Medical Devices companies.This is an FSP role - you will have the scientific exposure associated with activities developed in a global Pharma, while benefit from the remote flexibility coming from the CRO employment. As Lead Data Manager you will be responsible of all Data Management activities on project level, essentially you will take leadership on study level and ensure quality deliverables on time and within budget. You will act as SME - subject matter expert - and provide leadership and vision to the team, drive process standardisation and manage vendors.The successful candidate will have:- BSc in life sciences with minimum 3 years of DM experience within pharma sector; - End-to-end experience (from setting-up to delivering clean database locks);- Excellent communication skills - able to manage clients and internal teams;- Ability to work in a multicultural environment;- Proactive, team-oriented attitude;- RAVE experience would be a strong advantage;If you're looking to work with a global organization that will provide excellent development opportunities, this is the right opportunity for you! You will work close with some of the brightest individuals in life-changing projects helping and transforming the millions of patients out there. Don't hesitate and get in touch for a confidential chat about this Lead Data Manager role and please send your updated CV to:Catalin ZahariaSenior Consultant - BiometricsData Management, Statistical Programming, Biostatistics Tel: +44 (0) 207 255 66 10Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia
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Project Manager, Clinical Data Management
England |
£55000 - £65000 per annum + Bonus & benefits
Clinical Data Management, Project Manager Home Based in UK, Ireland or SpainA world recognized and highly innovative CRO are looking to appoint a highly experienced Clinical Data Manager, Project Manager to oversee and lead CDM projects in key, demanded therapeutic indications. This is a full time and permanent opportunity that will provide you with flexible working hours and a couple of days of remote flexibility on weekly basis.The company has extended reputation in key therapeutic indications e.g. oncology, rheumatology, rare diseases, etc. and has supported the development of most successful products. Through their particular focus on innovation and a consistent quality centric approach, they have secured a very stable team which are now growing further due to business needs.The role will be heavily focused on oversight and management of ongoing clinical studies, including external vendors associated with the trial. Key responsibilities:- Coordinate the project through timelines overview, database locks approval, monitoring progress of clinical projects and ensure delivery within the scope of timelines and budgets. - Lead and participate in the development and implementation on processes, policies and DM documentation.- Participate and lead DM and cross functional groups.- Promote a continuous improvement of DM in the wider scope of activity though training and education.- Manage, sponsors and external vendors on project level.You will have:- BSc in life sciences, IT or business administration.- Extended Clinical Data Management experience developed in clinical trials.- Previous oversight experience of vendors (CRO's, central labs, 3rd party vendors, etc.)- Knowledge of industry standards and processes.- Excellent communication skills.- Proactive, solution focused attitude.This is a great opportunity to join a company that has and continue the development of key products in the market in highly demanded therapeutic indications. Don't hesitate and get in touch for an informal and confidential chat about this Project Manager, Clinical Data Management role, alternatively send your CV to:Catalin ZahariaPrincipal Consultant - Life Sciences RecruitmentBiometrics - SAS Programming, Biostatistics, Data Management Tel: +44 (0) 207 255 66 10Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia#CDM #SDTM #EDC #RAVE #Medidata #clinicaltrials #CRO #Pharma #Biotech
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Associate Director, Statistical Programming - Europe
England |
€75000 - €85000 per annum + Bonus & Standard Benefits
Statistical Programming, Associate DirectorUK & Europe - home basedCompetitive package A scientific focused CRO is looking to appoint an Associate Director, Statistical Programming and work close with cross functions departments such as Biostatistics, Data Management and lead the biometrics operations within the business. This opportunity will be serving a technical experienced individual that would like to develop a strong and stable career in global business working close with an European based team.As Associate Director, Statistical Programming you will lead biometrics operations with related departments - Biostatistics, Statistical Programming, Data Management - and manage projects in clinical trials (from Phase I to submission). You will also functionally lead a team of experienced programmers and if needed will contribute with hands on tasks to meet the commitments.You will communicate with stakeholders the results, strategy and actively participate in developing tools and operational prototypes that will support the vision and strategy of the business.The successful candidate will have:* MSc in Computer Programming or Life Sciences - PhD would be preferred;* Minimum of 8 years of SAS Programming experience developed in Pharma/Biotech/CRO;* Strong clinical trials experience, ideally from phase I - III;* Extensive knowledge of CDISC standards and industry's regulation; * Strong communication skills with ability to adapt to different audiences;* SAS Certifications would be desired;* A structured mindset that will be reflected in work and communication.This is a fantastic opportunity to join a scientific focused CRO with great market longevity which has contributed to top selling products in the market in key therapeutic areas.If you looking to learn more about this Associate Director SAS Programming role with one of the most reputable and respected names in the industry, do not hesitate to get in touch for a confidential chat, alternatively send your CV to:Catalin ZahariaPrincipal Consultant - Life Sciences Biometrics - SAS Programming, Biostatistics, Data Management, Data AnalyticsTel: +44 (0) 207 255 66 65Catalin.zaharia@secpharma.comlinkedin.com/in/catalindoruzaharia
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Senior / Principal Biostatistician - Europe (home-based)
Italy |
€55000 - €75000 per annum
Fantastic opportunity to join one of the leader in clinical trials, supporting Global Pharma and Biotech.This position could be 100% Home based from UK/EUROPETo be successful in this role you will have the following profile: - MSc or PhD statistics, biostatistics, or related field - Demonstrated experience as a Statistician within a pharmaceutical, biotech or CRO environment - Experience developed across Phase I to IV studies - Strong SAS skills - Fluent in English (spoken and written) - Ability to work in team and independently - Previous experience with home based work is ideal If you are interested, reach out to me at : yanick.millet@secpharma.com with your CV updated and your best availability to set up a call.Yanick Millet Consultant - Life Sciences Recruitment Biometrics - SAS Programming, Biostatistics Tel: +44 (0) 207 255 66 00 - +33 (0) 1 70 80 74 89Email: yanick.millet@secpharma.com www.linkedin.com/in/yanick-millet-b6273b30/
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Senior/Principal Statistical SAS Programmer
England |
£55000 - £75000 per annum + High Benefits, Relocation Package
As an experienced Senior Statistician you will be expected to cover the following responsibilities: - Taking leadership of the statistical programming activities- Creating analysis datasets, tables, listing and figures from clinical trial data- Develop and validate analysis and reporting deliverables on the safety and efficacy side of programming- Collaborate effectively with an international team of programmers. Required Skills and Qualifications: - BSc in Computer Science, Applied Mathematics, Life Sciences or related fields; - Minimum 3 years of statistical programming in clinical trials - ideally in safety and efficacy + Leading Project.- Extended SAS Programming skills, including MACRO, Graphs, and TFLs - tables, figures and listings- Solid knowledge of the drug development cycle and related guidelines- Strong analytical mid-set with a particular focus on details- CDISC experience would be a massive advantage - Excellent communication skills in English, both verbal and writtenDo not hesitate to apply or contact me for more details about this role to: Yanick Millet Associate Consultant - Life Sciences Recruitment Biometrics - SAS Programming, Biostatistics Tel: +44 (0) 207 255 66 00 yanick.millet@secpharma.com
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Senior / Principal Biostatistician - Europe (home-based)
France |
€65000 - €75000 per annum + Bonus, Pension, Life Insurance
Fantastic opportunity to join one of the leader in clinical trials, supporting Global Pharma and Biotech.This position could be 100% Home based from UK/EUROPETo be successful in this role you will have the following profile: - MSc or PhD statistics, biostatistics, or related field - Demonstrated experience as a Statistician within a pharmaceutical, biotech or CRO environment - Experience developed across Phase I to IV studies - Strong SAS skills - Fluent in English (spoken and written) - Ability to work in team and independently - Previous experience with home based work is ideal If you are interested, reach out to me at : yanick.millet@secpharma.com with your CV updated and your best availability to set up a call.Yanick Millet Consultant - Life Sciences Recruitment Biometrics - SAS Programming, Biostatistics Tel: +44 (0) 207 255 66 00 - +33 (0) 1 70 80 74 89Email: yanick.millet@secpharma.com
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Manager - Team Lead Statistical Programming
Le Vaud |
Negotiable
Global Pharma is recruiting for a Team Lead Statistical Programming / ManagerResponsibilities:- Working as statistical programming lead- Responsible for all the relevant programming activities from SDTM to ADAM- Ensuring the oversight of external parties performing programming activities - Providing hands-on statistical programming support to clinical development, regulatory and market access submission- Supporting the submission team in response to regulatory agencies- Developing standard template on datasets and TFLs to improve efficiency and quality- Supporting the programming macros and tools for data review and monitoring, etc.Requirements:- BSc in a technical field such as computer science or mathematics; MSc in bio/statistics preferred- Minimum 5 years of proven experience within pharmaceutical life science industry or CROs- Expert in SAS macro and/or system utility development- Solid working experience of CDISC SDTM and ADaM, including implementation in clinical trials analysis- Proven experience of all phases of Human clinical trials, including interventional and non-interventional studies and submission- Extensive background of applied statistics- Proven experience of statistical methods using SAS- Solid understanding in database structures and set-up
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(Senior) Clinical Project Manager
London |
£60000 - £80000 per annum
I am currently seeking an individual to join a mid-size CRO as a Clinical Project Manager / Senior Clinical Project Manager (experience dependant) on a permanent basis. The CompanyThe company itself are more unique with their approach compared to others within the industry. They have more of a scientific and collaborative style to how they work with their Sponsors, working largely with organisations who may not necessarily have expertise in-house meaning that the company often take a lot of ownership of the development strategy of the product. The company has a modern office space in Central London and offer flexible home working options once office working returns. The RoleThe responsibilities of the role include, but are not limited to;* Management of all assigned global clinical studies from start-up through to close-out.* Oversight and cross-functional liaison across the company e.g. clinical teams, regulatory teams, biometrics teams etc.* Vendor and study budget management to ensure the timely and on-budget execution of all studies.* Managing and allocating work within the project team, ensuring members are performing all duties on time and in accordance to project requirements.* Preparation and representation of the company at bid defence meetings.The RequirementsThe requirements of the role include;* Minimum 3 years full service Clinical Project Management experience across multiple European countries.* Bachelors (or higher degree) in a life science related discipline.* Experience working within a CRO setting essential.* English fluency essential. If this opportunity sounds interesting to you then don't delay and apply today, or if you or someone you know wishes to have a confidential conversation regarding the position then send across a copy of your CV or give me a call using the contact details below.E: rebecca.law@SECpharma.comT: +44 (0)2072556620
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(Senior) Clinical Research Associate
England |
£35000 - £50000 per annum
I am currently seeking an individual to join an mid-size CRO in a permanent, home based position as a Clinical Research Associate II / Senior Clinical Research Associate (seniority level dependant on experience).The CompanyThe company itself are more unique with their approach compared to others within the industry. They have more of a scientific and collaborative style to how they work with their Sponsors, working largely with organisations who may not necessarily have expertise in-house meaning that the company often take a lot of ownership of the development strategy of the product.The RoleMain responsibilities include, but are not limited to;- Completing site selection, pre-study start up activities and assisting in site evaluation- Managing investigative site activity to ensure satisfactory study understanding and compliance of all site staff, and providing updates to the Study Manager as necessary- Assisting with study start-up or site management activities such as helping with regulatory submissions to Ethic Committees, contract negotiation and budget negotiation.- Completion of monitoring reports and follow-up letters; including all key findings and recommendations for future actions.- Maintaining Trial Master File (TMF)/electronic Trial Master File (eTMF).The PersonRequirements are as follows;- Minimum 2 years independent, on-site monitoring experience.- BSc in a Life Science related discipline (higher degrees very desirable).- Valid Drivers Licence.- Experience as CRA/Clinical Monitor in CRO/Pharma/Biotech essential.- Experience within complex therapies (e.g. oncology, neurology, rare diseases etc.) desirable.- Fluency in both English. If you are and established Clinical Research Associate looking for an exciting position with a reputable company then don't delay apply today or give me a call at +44 (0)20 7255 6620.If this isn't the role for you but you know someone that would be suitable, tell them to drop me an email or give me a call, I would love to hear from them!E: rebecca.law@SECpharma.comT: +44 (0)2072556620
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Senior Clinical Project Manager
England |
£60000 - £70000 per annum
I am currently seeking an experienced Clinical Project Manager to join a reputable CRO in a permanent, home based position as a Senior Clinical Project Manager.CompanyThe company itself is a small, full-service CRO with a growing European Clinical Operations team. The company has a extensive pipeline with key area's including oncology, CNS and rare disease, across both early and late stage development. A key focus for the company is to grow their operations in UK this year, so you would be one of the first key hires for their Clinical Operations team and would help to grow this division as the company continues to expand.RoleThe responsibilities of the role include, but are not limited to;* Management of all assigned clinical studies from start-up through to close-out at across Europe.* Oversight and cross-functional liaison across the company e.g. clinical teams, regulatory teams, biometrics teams etc.* Vendor and study budget management to ensure the timely and on-budget execution of all studies.* Managing and allocating work within the project team, ensuring members are performing all duties on time and in accordance to project requirements.RequirementsThe requirements of the role include;* Minimum 5 years full service Clinical Project Management experience across multiple European countries.* Bachelors (or higher degree) in a life science related discipline.* CRO experience preferred.* Monitoring background preferred.If this opportunity sounds interesting to you then don't delay and apply today, or if you or someone you know wishes to have a confidential conversation regarding the position then send across a copy of your CV or give me a call using the contact details below.E: rebecca.law@SECpharma.comT: +44 (0)2072556620
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Clinical Research Associate II
England |
£30000 - £43000 per annum
I am currently seeking experienced Clinical Research Associates to join a small CRO as a Clinical Monitor (Clinical Research Associate II)The CompanyThe organisation is a full-service European CRO who have an extensive pipeline of complex therapies (including rare diseases, CNS and haematology, to name but a few). They work with leading sponsors to provide multi-country clinical trials across all stages of development with established teams sitting in a multitude of European locations. With the UK identified as a key growth area for them there is plenty of scope for development within the role and the company as they continue to expand. The RoleResponsibilities include, but are not limited to;* Completing site selection, study start-up, interim monitoring and close-out visits independently.* Managing investigative site activity to ensure satisfactory study understanding and compliance of all site staff, and providing updates to the Study Manager as necessary* Completion of monitoring reports and follow-up letters.* Training of site staff and serve as main point of contact for all site investigative sites.* Maintaining Trial Master File (TMF)/electronic Trial Master File (eTMF).The PersonApplicant requirements include;* At least 18 months independent, on-site clinical monitoring experience within UK.* Minimum BSc in a life science related discipline (higher degrees very advantageous).* Fluency/professional working standard of both English. * Valid drivers licence.If this seems like an interesting opportunity then don't delay and apply today, or if you would prefer to have a confidential conversation regarding the role then send across a copy of your CV to the email address below or give me a call at +44 (0) 2072556620.If this opportunity is not right for you but you know someone who would be interested, tell them to get in touch!E: rebecca.law@SECpharma.comT: +44 (0) 2072556620
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HTA Statistician (Senior, Principal, AD) - Biopharma
England |
£50000 - £70000 per annum
- Oversee and contribute to HTA activities from a statistical perspective;- Develop statistical related documents, including statistical reports;- Participate and contribute to the department's strategy development.An exciting opportunity has become available as Associate Director, Statistics with a global Biopharma to be based in UK on permanent basis. The company is recognized for its warm, open minded working culture and development opportunities, as such they secured a top place in the industry.As HTA Statistician, you will actively contribute to statistical strategy on project level and work close with key departments such as Medical Affairs, Programming and Data Management. Your exposure will be focusing on medical affairs statistics with exposure also to clinical development, and be involved/oversee submissions with local authorities. The successful candidate will have:- MSc in Medical Statistics, Applied Mathematics, Life Sciences or related analytical fields; - Demonstrable experience with meta-analysis;- Solid experience in project leading from a statistical perspective;- Strong experience in HEOR / HTA / RWE;- Extended SAS OR R programming experience;- Excellent communication skills and ability to adapt to different audiences.If you are interested in learning more about this great opportunity, do not hesitate to get in touch at catalin.zaharia@secpharma.com or +44 (0)20 7255 6610
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Biostatistics Manager - Swiss Biotech
Switzerland |
- Coordinate statistical activities for clinical trials in both, design and reporting- Create project specific strategies and follow up the implementation- Provide leadership and support on individual level for team membersAn exciting opportunity has become available as Senior Manager, Statistics with a boutique Biopharma to be home based in Switzerland.As Statistics Senior Manager you will actively contribute to biostatistics strategy on project level and work on strategic, innovative products. Your exposure will be focusing on clinical trials, from phase 1 to 4, and will provide technical and statistical leadership with a global team.The successful candidate will have:MSc in Medical Statistics, Applied Mathematics, Life Sciences or related analytical fields; Solid experience in project leading Strong experience in clinical trials SAS or R programming experienceExcellent communication skills and ability to adapt to different audiencesIf you are interested in learning more about this great opportunity, do not hesitate to get in touch with Catalin on catalin.zaharia@secpharma.com or feel free to call him at +44 (0)20 7255 6600
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Senior Pharma SAS Programmer
London |
£45 - £50 per hour
Our leading client is looking for a Senior SAS programming contractor to join their team. This is a UK homebased role and will be deemed as Inside IR35.The role of Senior SAS Programmer Contractor Biometrics is to perform and/or coordinate SAS programming activities. At all times, the Senior SAS Programmer Contractor will ensure that all services are performed to the highest standards and within required timeframes and budgets. The Senior SAS Programmer Contractor will have an excellent level of technical SAS programming skills and will have excellent interpersonal skills with a flexible, pragmatic approach to identifying solutions to issues. Responsibilities*Reviews documents that have an impact on SAS programming*Performs SAS programming for efficacy and safety tables, listings, figures and analyses*Performs SAS programming for CDISC SDTM and/or ADaM datasets*Produces tables, listings and figures of data for reports (e.g. Clinical Study Reports, Statistical Reports, etc)*May produce CDISC associated files, such as Define.XML, reviewer's guides and SDTM annotated CRFs*May mentor other SAS Programmers Competencies*Excellent working knowledge of SAS, CDISC (both SDTM and ADaM) standards and other relevant software technologies*Excellent level of proficiency in the full range of essential SAS programming tasks *Knowledge of the pharmaceutical industry processes and regulations, with good understanding of clinical trials and the application of ICH GCP to SAS and SAS programming functions*Educated to Bachelor's or Master's degree level in a statistics or computing-related discipline*At least five years' experience of SAS programming within a pharmaceutical company or CRO*Previous experience in a CRO or consultancy is highly desirable.For further information please contact Nitin on +44 (0)207 255 6655 or via email at nitinw@secrecruitment.com
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Java Developer / Architect
Italy |
Negotiable
Location: Milan, ItalyWork Type: PermanentStart Date: ASAPPer conto di una realtà leader nell`ambito della consulenza, specializzata nei servizi di integrazione e implementazione di tecnologie più all'avanguardia per importanti aziende globali, cerchiamo per le sedi di Roma e Milano professionisti in ambito Java.In particolare siamo interessati ad entrare in contatto con candidati che abbiano una buona conoscenza di Java e che possediano le seguenti skills:-Java/Microservices Architect:Dai 2 ai 5 anni di esperienza nel design di enterprise architecture customizzate;Conoscenza dei pattern di design di IT software e architecture design;Esperienza su architetture basate su Java/J2EE e JavaScript e relativi framework, principali container technology;Conoscenza di database SQL e NoSQL, di premesse, topic, e pattern delle infrastrutture cloud, dei principali offering, componenti e vendor in ambito cloud (IaaS, PaaS, SaaS), metodologie e componenti DevOps, delle piattaforme Windows e UNIX.-Java Developer/Team Leader tecnico:Comprovata esperienza nello sviluppo di applicazioni IT e risultati finali durante il ciclo di vita dello sviluppo;Minimo due anni di esperienza nello sviluppo e nella progettazione con J2EE/JEE;Esperienza con metodologie Agile (Scrum, Kanban);Esperienza con JavaEE, Spring, Hibernate;Minimo 2 anni di esperienza con tecnologie web come HTML5, CSS3, AngularJS, JavaScript, JSON, Ajax, JQuery, Wicket.x .Completano il profilo le seguenti caratteristiche generali:Disponibilità a trasferteCertificazioni (rilevanti per l'area di focus)Buona conoscenza della lingua inglese scritta e parlataLaurea in informatica o in discipline tecnico scientifiche/ingegneristicheIl tuo ruolo sarà incentrato sull'esecuzione pro attiva e responsabile delle attività progettuali nelle quali sarai coinvolto. Sarai responsabile per la qualità del tuo lavoro e del suo pieno allineamento alle priorità, agli obiettivi e alle esigenze dei clienti.Queste sono posizioni a tempo indeterminato che offrono un'eccellente opportunità di partecipare come parte attiva ai diversi progetti. Se sei interessato a progredire nel tuo percorso di carriera e a lavorare per un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni.Per maggiori informazioni non esitare a contattarmi scrivendo a Blanca.Schintu@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Blanca.
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Salesforce Consultant/Developer
Italy |
Negotiable
Multiple Roles: SALESFORCE (BUSINESS ANALYST- DEVELOPER - SOLUTION ARCHITECT)Location: Roma e MilanoTipologia: Contratto a tempo indeterminatoInizio: ASAPPer conto di una realtà leader nell`ambito della consulenza, specializzata nei servizi di integrazione e implementazione di tecnologie più all'avanguardia per importanti aziende globali, cerchiamo profili funzionali e tecnici di varia seniority che operino nella programmazione, sviluppo e implementazione del CRM Salesforce.Business Analyst/ConsultantDeveloperSolution ArchitectManagerMarketing Automation Technical ConsultantIn particolare siamo interessati ad entrare in contatto con candidati che abbiano esperienza di almeno 2 anni e che nello specifico abbiano i seguenti requisiti:-BUSINESS ANALYST:Esperienza in tutte le industries, in particolare con esperienza su clienti del mondo Financial Services e Resources;Esperienza nella gestione dei progetti con metodologia Waterfall e Agile;Conoscenza dei prodotti e dei processi CRM (Salesforce, Siebel, CRM Dynamics, CRM SAP) in ambito di specifiche industry;-DEVELOPER:Preferibile conoscenza di Mulesoft;Disegno e realizzazione delle migliori soluzioni tecnologiche per soddisfare le esigenze del clienteConfigurazione della piattaforma Salesforce.com (Object Configuration, Standard layout composition, design Workflow, Process Builder, Approval Process, validation rule, ecc.);Sviluppo della piattaforma (classi Apex, pagine Visual Force, Lighting component, trigger, web services)-SOLUTION ARCHITECT :Preferibile conoscenza di Mulesoft + VlocityPreferibile esperienza su industry FSEsperienza nel disegno di architetture e mappe applicative nonché di integrazione dei sistemi per grandi aziendeOttima conoscenza dei principi di Data DesignOttima conoscenza dei principi di Integration Design -MANAGER:Esperienza come Project Manager/PMO in attività di governance di progetti SFDCEsperienza nella configurazione di Salesforce.com sales, service and/or marketing cloud.6+ anni esperienza nell'implementazione del CRMEsperto metodologia Agile -MARKETING AUTOMATION TECHNICAL CONSULTANT:6+ mesi di esperienza con Salesforce Marketing Cloud e le sue componenti Social Studio e Pardot o altri tool simili;Esperienza di almeno 6 mesi su attività di Marketing, Digital Marketing e Campaign Management su progetti multi-channelEsperienza con la piattaforma Salesforce CRMConoscenza dei linguaggi di programmazione front-end (HTML, CSS, Javascript, Jquery), dei database relazionali e di SQLConoscenza della DMPFamiliarità con la metodologia di progetto agile e/o semi-agile.Completano i profili le seguenti caratteristiche generali:Disponibilità a trasferteCertificazioni (rilevanti per l'area di focus)Buona conoscenza della lingua inglese scritta e parlataLaurea in informatica o in discipline tecnico scientifiche/ingegneristiche Queste sono posizioni a tempo Indeterminato che offrono un'eccellente opportunità di partecipare come parte attiva ai diversi progetti.Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni.Per maggiori informazioni non esitare a scrivere e inviare il CV a Blanca.Schintu@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Blanca.
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Release and Environment Manager
Cheltenham |
£60000 - £70000 per annum + Plus Benefits
Our leading International client, a global, manufacturer are currently searching for an experienced Release and Environments Manager to join their team and take responsibility for ensuring that there is a standardised and controlled release process and environments management process within the Delivery Lifecycle.The successful applicant will be responsible for designing, embedding and maintaining an effective release management and environments framework as well as co-ordinating and managing releases across a portfolio of IT assets with core business systems including: D365 CRM, Oracle's CPQ, Data Platform, Integration and Oracle JDE E1 9.2. The releases may include application updates and enhancements, platform upgrades and security improvements. You will be responsible for implementing and managing release processes and frameworks through development, test, and production environments. You'll work collaboratively across the business to ensure releases are delivered on schedule and within budget with minimal disruption to services.The role will also oversee a forward schedule of releases for BAU system upgrades and version changes, whilst supporting other technical experts across the business with large scale implementations using a current mix of Agile and Waterfall methodologies. The role will promote the discipline of Release & Environments Management across the business.The appointed candidate will be experienced in change, release and environment management, ideally with experience of working in a global environment. You'll bring great people engagement skills, knowledge of different delivery platforms, and a good understanding of good practice across project delivery, service delivery and awareness of devops.For further information please contact Nitin on +44 (0)207 255 6655 or via email at nitinw@secrecruitment.com
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Clinical Data Manager *2
England |
£50 - £55 per hour
Our leading client are looking for two Clinical Data Team Leads to join them on a contract basis.Contracts will be offered initially for 1 year and can be performed remotely from UK or the Continent.Role Description:Applies relevant components of the project protocol to daily tasks and directs others on how to apply to their daily tasks.* Acts as an interdepartmental and client liaison for all DM study activities.* Produces project-specific status reports for management, PM and/or clients on a regular basis.* Monitors and analyses study metrics and escalates per the organisation's risk management processes.* Participates in business development activities by assisting with bid preparation and representing data management at bid defence meetings, where required.* Assists with project forecasting of hours and identification of resource requirements.* Assists with the oversight of project budgets including identification of potential out of scope work and participation in the Contract Modification process.* Leads, high volume/highly complex studies.* Independently leads and delegates tasks to ensure timely completion of project activities to project timelines, quality and budget.* Mentors junior level staff on all associated tasks within a study.* Assists with administrative and financial oversight for allocated projects.* Communicates with managementWorks on problems of diverse scope where analysis of data requires evaluation of identifiable factors.Normally receives little instruction on day-to-day work, general instructions on new assignments. Demonstrates good judgement in selecting methods and techniques for obtaining solutions.Represents the department as a prime contact on projects. Interacts with internal and external personnel on significant matters often requiring coordination between functional areas. Networks with senior internal and external personnel in own area of expertise.Bachelor's degree or equivalent and relevant formal academic / vocational qualificationPrevious experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).Additional skills:* Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data* Strong customer focus and excellent interpersonal skills.* Ability to direct and train study team* Ability to act as a study or department expert for DM processes* Ability to support project resourcing and project timeline planning and adherence to timelinesFor further information please contact Nitin on +44 (0)207 255 6655 or via email at nitinw@secrecruitment.com
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iSeries Developer
Brussels, Belgium |
Up to €500 per day
The successful applicants will help develop and maintain transportation and customs declaration business requirements. The software engineer will assume an application development & maintenance role reporting to a Software Solutions team leader. His / her main task will be to investigate issues within the I- Series applications and/or be part of project teams developing new solutions.Requirements: - Good knowledge of English (verbal & written) is essential- 5 years' experience in software analysis & development on I-Series (medior)- thorough knowledge of SQL and RPG ILE (free) including embedded SQL- knowledge of XML, in general and in an RPG-context- knowledge of web services/SOAP in an RPG-context- knowledge of Stored Procedures- knowledge of I-Series methods: MQ series, FTP, DDM, IFS- I-Series Software Solutions experience with RPG/400 or older- familiarity with a software change management system, preferably ALDON Lm(i)- usage of IBM Rational- Ideally you will love commutable to the offices in Brussels.
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SAP SD Manager/Senior Manager
Milano, Milan |
Negotiable
SAP SD/MM Manager/Senior ManagerLocation: Milano/RomaTipologia: contratto a tempo indeterminatoInizio: ASAPAlcune delle società leader nel mercato consulenziale sono alla ricerca di svariati profili Manager e Senior Manager SAP SD su Milano o Roma.Requisiti:Persona con comprovata esperienza in progetti legati a SAP Logistics ( SD/MM/PP )Figura con un background funzionale su SAP SD.Potrai fare parte di un vivace network globale e di un team di persone impegnate in un continuo ampliamento delle proprie skills, offrendo ai Clienti Finali soluzioni di alto livello.Possiamo aprirti possibilità di carriera coinvolgendoti nella realizzazione di progetti importanti e all'avanguardia, grazie alla presenza globale dell'azienda.Queste sono posizioni a tempo indeterminato che offrono un'eccellente opportunità di partecipare come parte attiva ai diversi progetti.Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni.Per maggiori informazioni non esitare a scrivere e inviare il CV a federica.funari@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Federica.
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Servicenow Consultant (developer / analyst / manager)
Frome |
Negotiable
ServiceNow Consultant (developer / analyst / manager)Location: Milano - RomaTipologia: contratto a tempo indeterminato Inizio: ASAPUna delle più importanti e dinamiche aziende multinazionali di System Integration ricerca Consulenti Servicenow per le sue sedi di Milano e Roma.Avrai l'opportunità di operare all'interno di progetti prestigiosi e di alto valore tecnologico, in veste di sviluppatore, analista o consulente, fino alle figure manageriali, a seconda dell'esperienza maturata.Siamo interessati ad entrare in contatto anche con candidati che abbiano competenze di sviluppo (es AngularJS) e che siano interessati ad acquisire competenze e a crescere velocemente su una tecnologia in forte espansione come Servicenow.I requisiti:*Esperienza nell'implementazione e gestione di piattaforme di service management (ServiceNow, Bmc Remedy)*Minimo 6 mesi di esperienza nell'utilizzo di Javascript, Jquery, HTML o AngularJS*Competenze base in ITIL v3, SQLCerchiamo candidati dalla mente aperta, dinamici e proattivi, persone capaci di fare la differenza. Ti riconosci in questa descrizione?Potrai fare parte di un vivace network globale e di un team di persone impegnate in un continuo ampliamento delle proprie skills, offrendo ai Clienti Finali soluzioni di alto livello. Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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Frontend/Backend Developers
Milan, Milan |
Negotiable
Frontend/Backend Developer Location: Milano/RomaTipologia: contratto a tempo indeterminatoInizio: ASAPAlcune delle società leader nel mercato consulenziale è alla ricerca di svariati profili Frontend o Backend Developer per le sedi di Milano e RomaRequisiti:Persona con comprovata esperienza in progetti legati allo sviluppo Frontend di Angular/React o Backend su Java.Figura con un background tecnico su Angular/React o Java.Potrai fare parte di un vivace network globale e di un team di persone impegnate in un continuo ampliamento delle proprie skills, offrendo ai Clienti Finali soluzioni di alto livello.Possiamo aprirti possibilità di carriera coinvolgendoti nella realizzazione di progetti importanti e all'avanguardia, grazie alla presenza globale dell'azienda. Queste sono posizioni a tempo indeterminato che offrono un'eccellente opportunità di partecipare come parte attiva ai diversi progetti.Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a federica.funari@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Federica.
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Consulente SAP FI S/4 HANA
Milano, Milan |
Negotiable
SAP FI S/4 HANA *posizioni multiple per consulenti di diverse Seniority (Analyst / Consultant / Senior Consultant / Manager). Location: Milano, RomaTipologia: contratto a tempo indeterminato Inizio: ASAP Una delle più importanti e dinamiche aziende di System Integration ricerca consulenti SAP FI per diverse sedi in Italia. In seguito ad una forte crescita del business, in continua evoluzione, l'azienda cerca consulenti SAP FI con diversi livelli di esperienza nelle attività di analisi funzionale, customizing, implementazione e gestione di soluzioni applicative.La Societa' offre interessanti percorsi di carriera, rendendo disponibile un'ampia varietà di ruoli, a partire dal Business Analyst fino alle posizioni manageriali. In particolare siamo interessati ad entrare in contatto con consulenti in possesso di determinate caratteristiche:*Minimo 2 anni di esperienza*Esperienza di almeno 2 full implementation life cycles*Conoscenza approfondita di SAP S4HANA*Buona padronanza della lingua inglese, scritta e parlata*Disponibilita' a trasferte Per le posizioni di livello manageriale cerchiamo candidati che abbiano anche esperienza pregressa di: *Team management*Pre sales*Gestione di budget di progetto Completano il profilo: *Forte attitudine e propensione al team working*Problem solving Cerchiamo candidati dalla mente aperta, che siano in grado di proporre soluzioni innovative per i Clienti Finali, persone capaci di fare la differenza. Ti riconosci in questa descrizione?Potrai fare parte di un vivace network globale e di un team di persone impegnate in un continuo ampliamento delle proprie skills, offrendo ai Clienti Finali soluzioni di alto livello.Possiamo aprirti possibilità di carriera coinvolgendoti nella realizzazione di progetti importanti e all'avanguardia, grazie alla presenza globale dell'azienda, alle forti e longeve relazioni con i Clienti e grazie a una partnership strategica con il Vendor che da 40 anni consente di ideare e implementare le più innovative soluzioni di business. Queste sono posizioni a tempo indeterminato che offrono un'eccellente opportunità di partecipare come parte attiva ai diversi progetti.Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca Letizia.
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Medical and Payer Evidence Statistician * 4
England |
Up to £600 per day
Our leading International Pharmaceutical client are looking for 4 Medical and Payer Evidence statisticians to join them on a long term contract basis. The role will be initially based from home and in time from site.Key skills needed are:*Graduate degree in Statistics, Biostatistics, or related quantitative fields (epidemiology, health outcomes, health informatics or health economics) or equivalent course work/ technical experience with experience in pharma/healthcare or other relevant discipline.*MS with 5 years of experience or PhD with 2 years of experience in the design, analysis and reporting of clinical studies/trials in a pharmaceutical research or academic setting. *At least 3+ years-experience in RWE observational research study management and data analytics, either within pharmaceutical industry or with an observational research consulting firm or academia. *Extensive knowledge and demonstrated experience with a variety of real-world data sources and observational research study design/execution in biotech/pharmaceuticals, consulting or academia.For further information please contact Nitin on +44 (0)207 255 6655 or via email at nitinw@secrecruitment.com
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2* Statistical Programmers (Pharmaceutical)
England |
£55 - £60 per hour
Our leading Pharmaceutical client is looking for 2 experienced Statistical Programmers to join them on a contract basis. The roles are for 6 months and will be remote based from within the UK.You will have the following skills: *Strong Pharma / Healthcare / Bioscience background*At least 5 years experiences within a similar programming role (ideally 3+ years within Oncology)*Good knowledge and implement skills for CDISC standards*Strong SAS technical skills in creating SDTM/ADaM and TFLs*Good industry knowledge to independently perform the programming tasks with clinical study teams*Knowledge and experience of RECIST is advantageous but not mandatory.*Available within 4 weeksFor further information please contact Nitin on +44 (0)207 255 6655 or via email at nitinw@secrecruitment.com.
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Microservices Senior Application Developer
Naples, Naples |
Negotiable
Microservices Senior Application Developer Location: Napoli Tipologia: contratto a tempo indeterminato Inizio: ASAP Una delle più importanti e dinamiche aziende multinazionali di System Integration ricerca Senior Application Developer per microservizi.Cerchiamo candidati dalla mente aperta, dinamici e proattivi, persone capaci di fare la differenza. Ti riconosci in questa descrizione?Potrai fare parte di un vivace network globale e di un team di persone impegnate in un continuo ampliamento delle proprie skills, offrendo ai Clienti Finali soluzioni di alto livello. Avrai l'opportunità di operare all'interno di progetti prestigiosi e di alto valore tecnologico. Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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Pharmacovigilance and Epidemiology Manager
London |
Negotiable
Our leading Healthcare client are looking for a Manager Epidemiology to join them on a contract basis.The Manager role within the Department of Data Science & Biometrics/Epidemiology will contribute to the execution of Real World/observational research projects.The role:Contribute to or lead execution of observational research projects:Contribute to or lead the statistical analyses of observational studies and contribute to the interpretation of resultsContribute to the development and/or review of study protocols, statistical analysis plans and study reportsCommunicate scientific information to a variety of audiencesKey Duties and Responsibilities:Demonstrating a thorough knowledge of statistical programming principles, analysis methods and data resources in the field of Epidemiology and observational research utilizing industry-standard analytic toolsContribute to the preparation of study reports, conference abstracts and presentations, and manuscriptsSupport other intra-departmental and inter-departmental cross-functional activities to accomplish business objectivesReview, synthesize, and critique the published literature and generate (systematic) reviewsMay assess and implement new data resources, methods, technology and analytic toolsKnowledge, Experience and Skills:MPH/MSc or PhD in Epidemiology or Public Health or related field with significant experience in observational researchAdvanced knowledge of statistical methods and their application in observational researchAdvanced knowledge of statistical software packages (SAS and/or R)Analytic, problem-solving, and critical and creative thinking skillsExcellent attention to detail, teamwork and initiative, with flexibility to adapt to the needs of the organisation; maintain meticulous attention to project deadlinesExperience of working with large electronic health records/real world databasesFor further information please contact Nitin on +44 (0)207 255 6655 or via email nitinw@secrecruitment.com
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Front End Developer
Milano, Milan |
Negotiable
Front End Developer Location: Milano Tipologia: contratto a tempo indeterminato Inizio: ASAP Una delle più importanti e dinamiche aziende multinazionali di System Integration ricerca Sviluppatori Front End per la sua sede di Milano.I requisiti:*Diploma o Laurea in discipline tecnico-scientifiche*Esperienza di sviluppo in ambito Front-end*Esperienza lavorativa di minimo 1 anno su tecnologia React o Angular.*Forte orientamento all'obiettivo ed eccellenti capacità di analisi e sintesiCerchiamo candidati dalla mente aperta, dinamici e proattivi, persone capaci di fare la differenza. Ti riconosci in questa descrizione?Potrai fare parte di un vivace network globale e di un team di persone impegnate in un continuo ampliamento delle proprie skills, offrendo ai Clienti Finali soluzioni di alto livello. Avrai l'opportunità di operare all'interno di progetti prestigiosi e di alto valore tecnologico. Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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Java/Microservices Architect
Milano, Milan |
Negotiable
Microservices Solution ArchitectLocation: MilanoTipologia: contratto a tempo indeterminato Inizio: ASAPUna delle più importanti e dinamiche aziende multinazionali di System Integration ricerca IT Architect per la sua sede di Milano. Avrai l'opportunità di operare all'interno di progetti prestigiosi e di alto valore tecnologico.Farai parte di un gruppo di Consulenti coinvolto in importanti progetti innovativi per i clienti di tutti i settori. Avrai un accesso privilegiato e anticipato alle tecnologie di ultima generazione, grazie ad alleanze con i più importanti player del mercato digitale.Utilizzerai architetture e piattaforme Cloud per aiutare le più importanti aziende globali a trasformare velocemente le idee in applicazioni e servizi concreti.Il ruolo:Avrai la possibilità di gestire il design di soluzioni infrastrutturali e fornire un supporto all'implementazione di enterprise architecture basate su metodologie e pattern di ultima generazione: Microservices, Native Cloud, Serverless, PaaS e Container-based, Google Cloud Platform.Ricoprirai il ruolo di advisor e, grazie alla capacità di acquisire velocemente skill tecniche, potrai migliorare il business dei clientiI requisiti:*Una spiccata passione per l'innovazione e per la gestione di leading edge technology*Da 3 a 5 anni di esperienza nel design di enterprise architecture customizzate *Conoscenza dei pattern di design di IT software e architecture design *Competenza ed esperienza su architetture basate su Java/J2EE e JavaScript e relativi framework, principali container technology*Conoscenza di database SQL e NoSQL, di premesse, topic e pattern delle infrastrutture cloud, dei principali offering, componenti e vendor in ambito cloud (IaaS/PaaS/SaaS), dei vari componenti, utilizzi e paradigmi di integrazione, delle metodologie e le componenti DevOps, delle piattaforme Windows e UNIX*Ottima conoscenza dell'Inglese*Costituisce titolo preferenziale la conoscenza della suite di servizi Google Cloud PlatformCerchiamo candidati dalla mente aperta, dinamici e proattivi, persone capaci di fare la differenza. Ti riconosci in questa descrizione?Potrai fare parte di un vivace network globale e di un team di persone impegnate in un continuo ampliamento delle proprie skills, offrendo ai Clienti Finali soluzioni di alto livello. Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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Back End Java Developer Freelance
Milano, Milan |
Negotiable
Back End Java Developer - freelance3 mesi (con possibilità di estensione)******urgent contract******Tipo di contratto: a tempo determinatoDurata: fino al 31/12/2020 - full time Data di inizio: ASAPSede: Milano (inizialmente da remoto)Daily rate: competitivaUn importante Gruppo operante nella Consulenza Direzionale e nell'Information Technology ricerca un Java BE Developer a Milano, per un contratto della durata di 3 mesi.I requisiti: Cerchiamo risorse che abbiano maturato almeno 2 anni di esperienza di sviluppo e che abbiano le seguenti competenze:*Java developer Release >8 o equivalente openjdk*Conoscenza di Java entrprise edition da release 6*Conoscenza del design Object Oriented e dei pattern base*Framework open source più diffusi (Hibernate, JPA, Spring Boot, Spring Security, Spring Integration, Spring Data, Logback, Log4j, ecc) *Uno o più Application/web Server (WebSphere, Wildfly, Apache Tomcat, Bea Weblogic) *Conoscenza da sviluppatore dei maggiori database relazionali (Oracle, PostgreSql. Db2, Mysql)*Framework di integrazione Apache ActiveMQ e/o Apache Camel*Tool sviluppo eclipse-Gradita conoscenza UML con i principali diagrammi-Possibile precedente esperienza in batch e/o enterprise integration pattern-Gradita conoscenza progettazione e sviluppo in modalità Test Driven Development-Gradita una precedente esperienza agile (scrum/kanban)Questa è una posizione a tempo determinato che offre un'eccellente opportunità di partecipare come parte attiva in un contesto multinazionale e stimolante.Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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Java/Microservices Architect
Milano, Milan |
Negotiable
Java/Microservices Architect Location: Milano Tipologia: contratto a tempo indeterminato Inizio: ASAP Una delle più importanti e dinamiche aziende multinazionali di System Integration ricerca Architetti Java e di microservizi.I requisiti:*Dai 3 ai 5 anni di esperienza nel design di enterprise architecture customizzate;*Conoscenza dei pattern di design di IT software e architecture design;*Esperienza su architetture basate su Java/J2EE e JavaScript e relativi framework, principali container technology;*Conoscenza di database SQL e NoSQL, di premesse, topic, e pattern delle infrastrutture cloud, dei principali offering, componenti e vendor in ambito cloud (IaaS, PaaS, SaaS), metodologie e componenti DevOps, delle piattaforme Windows e UNIX.Cerchiamo candidati dalla mente aperta, dinamici e proattivi, persone capaci di fare la differenza. Ti riconosci in questa descrizione?Potrai fare parte di un vivace network globale e di un team di persone impegnate in un continuo ampliamento delle proprie skills, offrendo ai Clienti Finali soluzioni di alto livello. Avrai l'opportunità di operare all'interno di progetti prestigiosi e di alto valore tecnologico. Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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SAP Project Manager
Milan, Milan |
Negotiable
Siamo alla ricerca di figure professionali di livello Project Manager in ambito SAP, per conto di aziende leader nella consulenza informatica. Il candidato dovrà aver:- svolto la mansione di Project Manager in ALMENO UN progetto full life cycle dalla raccolta requisiti fino al post go-live- aver gestito relazioni commerciali e strategiche con i clienti ed i gruppi di lavoro- aver coordinato in autonomia le attività di delivery, dalla pianificazione dei tempi al budgeting- avere una conoscenza architetturale ed applicativa della piattaforma SAP con una profonda conoscenza degli scenari S/4HANA Cloud - preferibilmente aver maturato una consolidata esperienza nell' area funzionale SAP FI/CO- aver esperienza nella gestione di progetti SAP complessi articolati su diversi stream di lavoro, coordinando risorse interne e fornitori esterniRequisiti imprescindibili del candidato sono:- Commitment e forte orientamento agli obiettivi- Sviluppate capacità di comunicazione- Autorevolezza e propositività- Flessibilità, atteggiamento positivo e predisposizione alla mediazione- Capacità di motivare le risorse- Ottime capacità organizzative ed orientamento al raggiungimento del risultato- Predisposizione al lavoro in team in un contesto internazionale- Conoscenza della lingua inglese, sia parlata che scritta- Disponibilità a trasferte in Italia e all'esteroSede di lavoro: MilanoContratto: inserimento diretto a tempo indeterminatoDisponibilità: ASAPPer saperne di piu' o per applicare scrivi e/o invia il tuo cv a raffaele.arena@secrecruitment.com oppure telefona allo 00442072556655 e chiedi di parlare con Raffaele.
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Front End Developer Senior
Milano, Milan |
Negotiable
Front End Developer Senior - freelance3 mesi******urgent contract in Milan******Tipo di contratto: a tempo determinatoDurata: 3 mesi: fino al 31/12/20Data di inizio: ASAPSede: Milano (Non sono previste trasferte)Daily rate: competitivaUn'importante Gruppo operante nella Consulenza Direzionale e nell'Information Technology ricerca un Front End Developer Senior a Milano, per un contratto della durata di 3 mesi.I requisiti: Cerchiamo risorse che abbiano maturato le seguenti competenze:-HTML5, CSS3, XML, NodeJS-Buona conoscenza della lingua IngleseCostituiscono titolo preferenziale la conoscenza di: ReactJS, Redux, ReactNative. Questa è una posizione a tempo determinato che offre un'eccellente opportunità di partecipare come parte attiva in un contesto multinazionale e stimolante.Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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Android Developer
Frome |
Negotiable
Android Developer - freelance3 mesi******urgent contract in Rome******Tipo di contratto: a tempo determinatoDurata: 3 mesi: fino al 31/12/20Data di inizio: ASAPSede: Roma (Non sono previste trasferte)Daily rate: competitivaUn'importante Gruppo operante nella Consulenza Direzionale e nell'Information Technology ricerca un Android Developer a Roma, per un contratto della durata di 3 mesi.Il ruolo:Parteciperai alla fase di disegno dell'architettura tecnica di Front End. I requisiti: Cerchiamo risorse che abbiano maturato le seguenti competenze:-Sviluppatore Android nativo (preferenziale conoscenza Kotlin)-Esperienza 3+ anni comprovati su progetti Android NativoCostituisce titolo preferenziale l'esperienza su Xamarin.Android. Questa è una posizione a tempo determinato che offre un'eccellente opportunità di partecipare come parte attiva in un contesto multinazionale e stimolante.Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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React JS Developer
Turin, Turin |
Negotiable
ReactJs Developer freelance3 mesi******urgent contract******Tipo di contratto: a tempo determinatoDurata: 3 mesi - fino al 31/12/2020 Data di inizio: ASAP Sede: Torino o remotoDaily rate: competitivaUn'importante Gruppo operante nella Consulenza Direzionale e nell'Information Technology ricerca un ReactJs Senior Developer and Architect per un contratto della durata di 3 mesi.Il ruolo:Work as frontend developer wihtin Industrial IoT context in order to develop Human Machine Interface to allow the interaction between users and industrial equipments. The solution is based on a modular architecture using React.js and well-known workflow frameworks as Redux.I requisiti:*3+ years experience on frontend development, Javascript, DOM manipulation and Javascript object model *1+ years experience on ReactJs and Redux *3+ years on RESTful API *1+ year with Bootstrap framework *Experience with common front-end development tools such as Babel, Webpack, NPM, etc.Queste sono posizioni a tempo determinato che offrono un'eccellente opportunità di partecipare come parte attiva in un contesto multinazionale e stimolante.Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, queste opportunità sono certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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React JS Senior Developer and Architect
Turin, Turin |
Negotiable
ReactJs Senior Developer and Architect freelance3 mesi******urgent contract******Tipo di contratto: a tempo determinatoDurata: 3 mesi - fino al 31/12/2020 Data di inizio: ASAP Sede: Torino o remotoDaily rate: competitivaUn'importante Gruppo operante nella Consulenza Direzionale e nell'Information Technology ricerca un ReactJs Senior Developer and Architect per un contratto della durata di 3 mesi.Il ruolo:Work as frontend developer wihtin Industrial IoT context in order to develop Human Machine Interface to allow the interaction between users and industrial equipments. The solution is based on a modular architecture using React.js and well-known workflow frameworks as Redux.I requisiti: *5+ years experience on frontend development, Javascript, DOM manipulation and Javascript object model *3+ years experience on ReactJs and Redux *5+ years on RESTful API *3+ year with Bootstrap framework *Experience with common front-end development tools such as Babel, Webpack, NPM, etc.Queste sono posizioni a tempo determinato che offrono un'eccellente opportunità di partecipare come parte attiva in un contesto multinazionale e stimolante.Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, queste opportunità sono certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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.Net Core Developer
Turin, Turin |
Negotiable
.Net Core Developer freelance3 mesi - Torino******urgent contract in Torino******Tipo di contratto: a tempo determinatoDurata: 3 mesi - fino al 31/12/2020 Data di inizio: ASAP Sede: Torino o remotoDaily rate: competitivaUn'importante Gruppo operante nella Consulenza Direzionale e nell'Information Technology ricerca un .Net Core Developer per un contratto della durata di 3 mesi a Torino.Il ruolo:Perform as software developer within Industrial IoT context. The solution is based on a containerized microservices architecture developed with .NET Core 3.1 framework. The solution will take care to integrate and manage industrial equipments to support production on-site.I requisiti: *1+ years experience on microservices architecture*1+ years experience on .NET Core and C# development *1+ years experience on database management *1+ years experience on container orchestration (example: Kubernetes, OpenShift) *2+ years experience on event driven solutions, Rest API - Knowledge of RPC framework (gRPC)Questa è una posizione a tempo determinato che offre un'eccellente opportunità di partecipare come parte attiva in un contesto multinazionale e stimolante.Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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SAS Programmers * 3
England |
£350 - £400 per day
Our leading International pharmaceutical client are looking for 3 experienced Contract SAS Developers to join them on a Data preparation project. The role can be performed remotely from elsewhere in the UK.You will need the following skills:*SAS Base and Macro experience. *Attention to details and precision.*Good communication skills (clear communication, collaboration, pro-activity, experienced in providing and receiving feedback).Good organization of work (meeting timelines, highlighting potential or real problems, process improvements).Additional Information: The task does not require anonymization, only:- Identify subjects who withdrew consent based on guideline and data sets provided- Identify key variables related to subject ID and country- Configure existing SAS programs to remove data from subjects who did not give or withdrew consent, or are from excluded country- If in validator role: compare double-programmed data vs production output (validation process might change in the future)For further information please contact Nitin on +44(0)207 255 6655 or via email at nitinw@secruitment.com
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Salesforce Marketing Cloud Consultant
Italy |
Negotiable
SALESFORCE Marketing Cloud Consultant Location: Milano, RomaTipologia: Contratto a tempo indeterminato Inizio: ASAP Il tuo ruolo sarà incentrato sull' esecuzione proattiva e responsabile delle attività progettuali nelle quali sarai coinvolto. Con la supervisione dei colleghi più esperti, sarai responsabile per la qualità del tuo lavoro e del suo pieno allineamento alle priorità, agli obiettivi e alle esigenze dei clienti.Per una piena copertura del tuo ruolo, dovrai in particolare essere in grado di: -Collaborare con il team di progetto in modo proattivo e collaborativo -Comunicare in modo chiaro e strutturato idee e proposte; -Essere costantemente focalizzato sul risultato, sulla responsabilità individuale e sulla qualità del lavoro; -Implementazione del flusso di lavoro di Marketing Cloud -Configurazioni, costruzioni e test dei percorsi o automazioni in base ai progetti proposti -Possedere un forte orientamento al team working, alla collaborazione e al supporto dei colleghi, mantenendo sempre un approccio positivo alle situazioni.In particolare siamo interessati ad entrare in contatto con candidati che abbiano almeno un anno di esperienza nell'implementazione di Salesforce.I requisiti:-Esperienza nella progettazione di soluzioni marketing (raccolta dei requisiti, valutazione delle capacità, progettazione)-Esperienza nella gestione delle campagne utilizzando Salesforce Marketing Cloud.-Ottime capacità analitiche e di problem solving-Orientamento al risultato e al cliente-Forte attitudine e propensione al team working-Disponibilita' a trasferteSono gradite, ma non indispensabili, le seguenti competenze:-Certificazioni Salesforce (Admin, Sales and Service Cloud Consultant) -Laurea -Buona conoscenza della lingua ingleseQueste sono posizioni a tempo Indeterminato che offrono un'eccellente opportunità di partecipare come parte attiva ai diversi progetti. Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a Blanca.Schintu@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Blanca.
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Trial Data Manager
Switzerland |
€600 - €650 per day
Our leading International client are looking for an experienced Trial Data Manager to join them on an initial 1 year contract basis from their offices near Basel in SwitzerlandThe role:*Ensures that Data Management (Biometry) activities (related to assigned study) adhere to Client Standards, and applicable regulations*Meets study timelines in terms of Data Management deliverables*Ensures data handling consistency within allocated study(ies)*Leads Data Management activities for assigned study*Provides Data Management input to the development of the study protocol*Coordinates the development of the (e)CRF in line with Client standards*Writes all study Data Management documents covering specifications for external data transfer, data cleanings and review tools that will be further provided to Data Management Programmer(s) for development for the allocated study(ies)*Organizes, monitors and tracks the testing of data entry screens (eCRF layout), data cleaning / review tools, and their implementation in the production environment*Organizes, monitors and tracks data cleaning, data review, query management, and database lock. Makes sure processes are driven in collaboration with key Clinical Development (CD) stakeholders*Generates study metrics and status reports*Represents Data Management at Clinical Trial Team (CTT) meetings*Manages and is accountable for Data Management activities in studies where Data Management is outsourced (insourcing/outsourcing partners' management)*Prepares and archives Data Management study documentation Experience / Skills required: *Recognized degree in life sciences, mathematics, statistics, informatics or related disciplines*At least 3 years' experience in Pharmaceutical or Biotech industry within Clinical Research and / or Clinical*Data Management with good level of functional expertise in Data Management*Good knowledge of international clinical research regulations and requirements (e.g., International Conference on Harmonization - Good Clinical Practice (ICH/GCP))*Experience in clinical trial databases and applications, clinical data flow, data review, and (e)Case Report Form (CRF) design*Ability to lead and coordinate the activity of Data Manager(s) allocated to his/her study*Fluent in written and spoken English*For further information please contact Nitin on +44 (0)207 255 6655 or +41 (0)44 580 3717 or via email at nitinw@secrecruitment.com
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Data Warehouse Architect / Project Lead
England |
Negotiable
Our leading International client are looking for a Data Warehouse Architect to help assist on their global project.This is a 6 month initial contract remotely based out of the UK.Key Requirements:Project Leading / Management skills.Data Warehouse Architect experienceAbility to communicate with primary stakeholders.Requirement GatheringDocumenting Requirements Discussing requirements with the technical teamManaging the project forwards towards the goal of producing the required outputsExperience of a "Star Schema Data Warehouse"Technical environment:Oracle and MS/SQLETL: tSQL with additional SQL Server Integration ServicesReporting tool: PowerBIData Warehouse Platform: SQL server 2019For further information please contact Nitin on +44 (0)207 255 6655 or via email at nitinw@secrecruitment.com
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Oracle Database Adminstrator
Brussels, Belgium |
€500 - €550 per day
Our leading International client are looking for an experienced Oracle DBA on a contract basis from their offices in Brussels.You will have a minimum of 3 years experience as an Oracle DATABASE Administrator. Your role will be to continuously deliver technical implementation and provide 2nd line operational support including monitoring. You will also support business initiatives at both Global and Regional level. More specifically your role will be to:* Take part in technical projects in given area of expertise, such as Operating System, Database, Middleware, or infrastructure applications. You will Implement and deploy new Oracle Databases while making sure you are aligned with the provided infrastructure standards and remain within the project plan/objectives.* Provide 2nd level technical support to internal and external customers (Global Aviation, EAT, Hubs & Gateways, Aviation Management Team) and mentoring to more junior system engineers to ensure all technical issues and escalations are successfully resolved and that all emergency fixes/changes are appropriately documented and implemented.* Implement solutions which are scale able, supportable and aligned with global standards and industry best demonstrated practices.* During the above you will ensure customer satisfaction and compliance with the agreed SLA's.We are looking for:* Contractor that easily breaks down problems and situations into the different components and identify the gaps to acquire a clear understanding of the problem/situation to create solutions and remedies.* Strong understanding of customer needs and always taking these into consideration when taking actions or making decisions.* Strong communication skills. * A good team player who knows how to cooperate with others to achieve the common goals and know how to create and sustain effective relationships with colleagues and customers.* A minimum of 5 years experience in IT and Oracle DB management and ideally in IT enterprise environments.The role will be a contract in Belgium and thus you will need to work via a Belgian Umbrella company or your own Belgian company.For further information please contact Nitin on +44 (0) 207 255 6655 or via email at nitinw@secrecruitment.com
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Java BE Developer - freelance
Milano, Milan |
Negotiable
Java BE Developer - freelance9 mesi******urgent contract******Tipo di contratto: a tempo determinatoDurata: da 01/09/2020 a l 06/06/2021 - full time Data di inizio: 01/09/2020 Sede: MilanoDaily rate: competitivaUn'importante Gruppo operante nella Consulenza Direzionale e nell'Information Technology ricerca un Java BE Developer a Milano, per un contratto della durata di 6 mesi.Il ruolo:Ti occuperai di gestire attività di sviluppo end-to-end, recepirai I requisiti funzionali, scriverai le analisi tecniche e svilupperai microservizi in linguaggio Java.I requisiti: Cerchiamo risorse che abbiano maturato almeno 3 anni di esperienza di sviluppo e che abbiano le seguenti competenze:-Java BE-Microservizi in Java-Capacità di sviluppo end-to-end con scrittura analisi tecnica.Questa è una posizione a tempo determinato che offre un'eccellente opportunità di partecipare come parte attiva in un contesto multinazionale e stimolante.Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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Java Developer - freelance
Milano, Milan |
Negotiable
Java Developer - freelance6 mesi******urgent contract in Milan******Tipo di contratto: a tempo determinatoDurata: 6 mesi: da 01/09/20 a 28/02/2021 - full time Data di inizio: 01/09/20Sede: MilanoDaily rate: competitivaUn'importante Gruppo operante nella Consulenza Direzionale e nell'Information Technology ricerca profili Application Developer Java a Milano, per un contratto della durata di 6 mesi.Il ruolo:Parteciperai ad un progetto di trasformazione digitale. I requisiti: Cerchiamo risorse con almeno 4 anni di esperienza, che abbiano maturato le seguenti competenze:-Java, framework Spring e protocollo Rest-Sviluppo Java back enf e front end su ambiente microservizi Questa è una posizione a tempo determinato che offre un'eccellente opportunità di partecipare come parte attiva in un contesto multinazionale e stimolante.Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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Seniorn Consultant SAP FM - Freelance
Frome |
Negotiable
Senior Consultant SAP FM freelance16 mesi******urgent contract******Tipo di contratto: a tempo determinatoDurata: fino a fine 2021 - full time Data di inizio: ASAP Sede: da remoto con massima disponibilità a recarsi presso il cliente a RomaDaily rate: competitivaUn'importante Gruppo operante nella Consulenza Direzionale e nell'Information Technology ricerca Senior Consultant / Senior Matter expert con competenze di contabilità finanziaria della Pubblica Amministrazione e del modulo SAP Funds Management (SAP FM) per un contratto che avrà durata fino a fine 2021.Il ruolo:L'attività di cui ti occuperai è l'analisi, il disegno, la realizzazione, il test, il deploy e la documentazione di task specifici nella soluzione di contabilità finanziaria dello Stato sul modulo SAP FM. Ci sarà anche la possibilità di erogare corsi sulle tematiche direttamente gestite e di predisporre la relativa documentazione a supporto degli stessi.I requisiti: Cerchiamo risorse con esperienza pratica sul sistema e volontà a lavorare anche sull'implementazione del sistema. La capacità di relazionarsi con il cliente è requisito imprescindibile.Questa è una posizione a tempo determinato che offre un'eccellente opportunità di partecipare come parte attiva in un contesto multinazionale e stimolante.Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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Zuora Billing Expert
Milan, Milan |
Negotiable
Job Title: Senior Billing DeveloperExperience: Mid levelJob Function: Senior Billing DeveloperEmployment Type: Full-timeJob Description:This position will act as a full stack Billing Developer within the B/OSS delivery team.and the candidate will be primarily responsible for development of Zuora Platform.The candidate will display a growing proficiency in development, maintenance and support of multiple core software systems within the team product catalogue.The candidate will work at customer site or from Milan office on the following activities:· Design Integrated Billing Architectures· Design Billing solution according to Platform Best Practise· Project and Activities ManagementHe/she will be able to:· Understand client need and address them· Translate business needs into technical solution· Design and delivering tailored solutions involving, out-of-the-box features,· Configure catalog items, pricing, billing, and provisioning configurations· Provide status update· Advise customer executives with the best cost effective solutions· Interact with colleagues and contribute to their professional developmentDesired Skills and ExpertiseCandidate must be familiar with Billing integrated solution in complex enterprise Architecture.Should have:· 3+ years of experience as Zuora or Oracle BRM or Sap Hybris Billing Developer· Deep experience of integrating Billing Platform with other enterprise systems· Experience in Billing configurations for rating, product catalog, real time rating, Accounts Receivable, Payment Handling· Experience on Pipeline Batch Rating, Billing, Invoicing and Bill Cycle Management· Knowledge of Web services· Capability to write design documents, release notes, unit test cases· Capability to perform infrastructure related activities such as scripting/automation for setting up environments/testing automation/reporting automation.· To document requirements clearly and concisely, to author technical documents with design and integration details· To understand both Agile (SCRUM) and Waterfall delivery models, importance ofSDLC (Software Development Lifecycle Principles) and Cloud development best practicesIn addition:- Good relationship skills / Customer oriented- Team player- Flexibility and problem solving attitudeThe desire candidate has 1+ years of experience as Billing Developer, is motivated and fresh minded, customer oriented and with an excellent team spirit.
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SAP FI
Milano, Milan |
Negotiable
Project Manager SAPRole descriptionNTT DATA Italia sta cercando un "Project Manager SAP " per la propria sede di Milano.Si richiede una esperienza documentata superiore agli 8 anni nella implementazione di soluzioni SAP e l'aver ricoperto il ruolo di Project Manager in almeno un progetto end-to-end, dalla fase di start-up al go-live e post go-live.Il candidato/la candidata sarà il punto di raccordo tra chi gestisce la relazione commerciale e strategica con il cliente ed il gruppo di lavoro, di cui dovrà coordinare in autonomia le attività di delivery, inclusa la pianificazione dei tempi ed il controllo dei costi. Dovrà inoltre garantire la coerenza e la consistenza funzionale e tecnica della soluzione proposta e implementata.Required SkillsSi richiede una consolidata esperienza nella gestione di progetti SAP complessi articolati su diversi stream di lavoro, la capacità di coordinare team distribuiti sul territorio costituiti da risorse interne e terze parti, nonché la conoscenza di metodologie di project management tradizionali e agile.Requisito indispensabile è una ottima conoscenza architetturale ed applicativa della piattaforma SAP ed una maturata consapevolezza degli scenari S/4HANA Cloud.Si richiede inoltre preferibilmente una consolidata competenza nell'area funzionale/di processo amministrazione-finanza-controllo (SAP FI/CO).Costituiscono infine elementi qualificanti del profilo ricercato la predisposizione alla relazione interpersonale e la capacità di interagire in modo efficace e costruttivo con il cliente finale a vari livelli e con i colleghi.Requisiti indispensabili a completamento del profilo sono:- Commitment e forte orientamento agli obiettivi- Sviluppate capacità di comunicazione- Autorevolezza e propositività- Flessibilità, atteggiamento positivo e predisposizione alla mediazione- Capacità di motivare le risorse- Ottime capacità organizzative ed orientamento al raggiungimento del risultato- Predisposizione al lavoro in team in un contesto internazionale- Conoscenza della lingua inglese, sia parlata che scritta- Disponibilità a trasferte in Italia e all'estero
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Salesforce Project Lead
Milano, Milan |
Negotiable
Project LeadPersona con comprovata esperienza in progettilegati all'ambito CRM con un backgroundtecnico che garantista la lead di un progetto siain termini di interfacciamento con il businessche di conduzione di un team di lavoroKeyword competenze: Salesforce/Siebel/Microsoft DynamicsSeniority indicativa (in anni) 4+ anni
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Mulesoft Developer - Integration Specialist
Milano, Milan |
Negotiable
Mulesoft Developer - Integration Specialist / Sviluppatori per reskilling su Mulesoft Location: Roma - MilanoTipologia: contratto a tempo indeterminato Inizio: ASAP Una delle più importanti e dinamiche aziende multinazionali di System Integration offre interessanti opportunità Mulesoft, su Roma e Milano.In particolare siamo interessati ad entrare in contatto con candidati che: A.Abbiano maturato minimo 2 anni di esperienza nello sviluppo MulesoftB.Oppure che desiderino ampliare la propria esperienza acquisendo competenze Mulesoft con un reskilling sulla tecnologia, e che siano in possesso di almeno una delle seguenti competenze:1.Tibco2.Oracle SOA3.Boomi4.Informatica5.WSO26.Jboss ESB7.Red Hat Fuse8.Mule ESB Completano il profilo:*Ottime capacità analitiche e di problem solving*Orientamento al risultato*Orientamento al cliente*Forte attitudine e propensione al team working Cerchiamo candidati dalla mente aperta, dinamici e proattivi, persone capaci di fare la differenza. Ti riconosci in questa descrizione?Potrai fare parte di un vivace network globale e di un team di persone impegnate in un continuo ampliamento delle proprie skills, offrendo ai Clienti Finali soluzioni di alto livello. Avrai l'opportunità di operare all'interno di progetti prestigiosi e di alto valore tecnologico. Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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JAVA Developer / Team Leader
Milano, Milan |
Negotiable
Java Developer / Team leader Location: Milano, RomaTipologia: contratto a tempo indeterminato Inizio: ASAP Una delle più importanti e dinamiche aziende multinazionali di System Integration ricerca Team Leader Java per diverse sedi in Italia.I requisiti:*Comprovata esperienza nello sviluppo di applicazioni IT e risultati finali durante il ciclo di vita dello sviluppo;*Minimo due anni di esperienza nello sviluppo e nella progettazione con J2EE/JEE;*Esperienza con metodologie Agile (Scrum, Kanban);*Esperienza con JavaEE, Spring, Hibernate;*Minimo 2 anni di esperienza con tecnologie web come HTML5, CSS3, AngularJS, JavaScript, JSON, Ajax, JQuery, Wicket.x .Cerchiamo candidati dalla mente aperta, dinamici e proattivi, persone capaci di fare la differenza. Ti riconosci in questa descrizione?Potrai fare parte di un vivace network globale e di un team di persone impegnate in un continuo ampliamento delle proprie skills, offrendo ai Clienti Finali soluzioni di alto livello. Avrai l'opportunità di operare all'interno di progetti prestigiosi e di alto valore tecnologico. Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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Front End Developer
Milano, Milan |
Negotiable
Front End Developer Location: Milano Tipologia: contratto a tempo indeterminato Inizio: ASAP Una delle più importanti e dinamiche aziende multinazionali di System Integration ricerca Sviluppatori Front End per la sua sede di Milano.I requisiti:*Diploma o Laurea in discipline tecnico-scientifiche*Esperienza di sviluppo in ambito Front-end*Esperienza lavorativa di minimo 1 anno su tecnologia React o Angular.*Forte orientamento all'obiettivo ed eccellenti capacità di analisi e sintesiCerchiamo candidati dalla mente aperta, dinamici e proattivi, persone capaci di fare la differenza. Ti riconosci in questa descrizione?Potrai fare parte di un vivace network globale e di un team di persone impegnate in un continuo ampliamento delle proprie skills, offrendo ai Clienti Finali soluzioni di alto livello. Avrai l'opportunità di operare all'interno di progetti prestigiosi e di alto valore tecnologico. Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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TIBCO Developer / Architect
Milano, Milan |
Negotiable
TIBCO Developer/Architect Location: Milano, Roma Tipologia: contratto a tempo indeterminato Inizio: ASAP Una delle più importanti e dinamiche aziende multinazionali di System Integration ricerca Sviluppatori Tibco su diverse sedi in Italia, che abbiano maturato almeno 2 anni di esperienza.Cerchiamo candidati dalla mente aperta, dinamici e proattivi, persone capaci di fare la differenza. Ti riconosci in questa descrizione?Potrai fare parte di un vivace network globale e di un team di persone impegnate in un continuo ampliamento delle proprie skills, offrendo ai Clienti Finali soluzioni di alto livello. Avrai l'opportunità di operare all'interno di progetti prestigiosi e di alto valore tecnologico. Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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Test Engineer (I-Series)
Brussels, Belgium |
€400 - €500 per day
Our leading International client are looking for an experienced AS/400 Test Engineer to join their team on a contract basis.The Role:In an international environment, the test engineer will be integrated in the current development & support team, some 30 people strong.The team develops and maintains in-house solutions on IBM I-Series for their international transportation and customs declaration business requirements.The Test Engineer will be responsible for producing test cases (both manual and automated), as well as executing tests and coordinating test related activities during the project life cycle.He/she support teams in unit/unit integration testing and offers guidance in regards to User Acceptance testing.The test-engineer will need to hit the ground running with minimal supervision and have the ability to work on multiple projects.Requirements:- A proven track record as a Test Engineer, especially experience with E2E testing.- Good knowledge of test case preparation, execution, requirements traceability and defect resolution.--Working knowledge of Tricentis Tosca Commander is highly desirable- Competent in using test tools such as HPQC/Jira- Have a thorough knowledge of structured test methods and processes- Have an eye for detail, with the ability to identify risks and grasp concepts quickly- Demonstrate the ability to communicate in a clear, simple, unambiguous and well structured manner and to have confidence in dealing with all levels across ourbusiness- IBM AS/400 (i-Series) knowledge is a strong benefitgood communication skills- Good analytical skills- Good knowledge of English (verbal & written) is essentialFor further information please contact Nitin on +44(0)207 255 6655 or via email at nitinw@secrecruitment.com
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Senior IT Developer Multipiattaforma/IT Architect
Milano, Milan |
Negotiable
Senior IT Developer Multipiattaforma/IT Architect Location: MilanoTipologia: contratto a tempo indeterminato Inizio: ASAP Una delle più dinamiche aziende di System Integration ricerca Sviluppatori e Architect per la sua sede di Milano.Il ruolo:Sarai inserito in progetti altamente innovativi.Il candidato ideale è un laureato in discipline tecnico-informatiche brillante, curioso e appassionato delle nuove tecnologie con almeno 5 anni di esperienza in progetti basati su:*Backend: JAVA, .NET C#, Python, PHP*Frontend: framework di sviluppo quali vue.js, react, angular*DB relazionali e linguaggio SQLCerchiamo candidati dalla mente aperta, dinamici e proattivi, persone capaci di fare la differenza. Ti riconosci in questa descrizione?Potrai fare parte di un vivace network globale e di un team di persone impegnate in un continuo ampliamento delle proprie skills, offrendo ai Clienti Finali soluzioni di alto livello. Avrai l'opportunità di operare all'interno di progetti prestigiosi e di alto valore tecnologico. Se sei interessato a progredire nel tuo percorso di carriera e a lavorare in un'azienda di dimensioni multinazionali, questa opportunità è certamente in linea con le tue aspirazioni. Per maggiori informazioni non esitare a scrivere e inviare il CV a francesca.letizia@secrecruitment.com o chiamando il +44 (0) 2072556655 e chiedendo di Francesca.
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iSeries Developer *2
Brussels, Belgium |
Negotiable
The successful applicants will help develop and maintain transportation and customs declaration business requirements. The software engineer will assume an application development & maintenance role reporting to a Software Solutions team leader. His / her main task will be to investigate issues within the I- Series applications and/or be part of project teams developing new solutions.Requirements: - Good knowledge of English (verbal & written) is essential- 5 years' experience in software analysis & development on I-Series (medior)- thorough knowledge of SQL and RPG ILE (free) including embedded SQL- knowledge of XML, in general and in an RPG-context- knowledge of web services/SOAP in an RPG-context- knowledge of Stored Procedures- knowledge of I-Series methods: MQ series, FTP, DDM, IFS- I-Series Software Solutions experience with RPG/400 or older- familiarity with a software change management system, preferably ALDON Lm(i)- usage of IBM Rational- Ideally you will love commutable to the offices in Brussels.
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ISeries Developer *2
Brussels, Belgium |
Negotiable
The successful applicants will help develop and maintain transportation and customs declaration business requirements. The software engineer will assume an application development & maintenance role reporting to a Software Solutions team leader. His / her main task will be to investigate issues within the I- Series applications and/or be part of project teams developing new solutions.Requirements: - Good knowledge of English (verbal & written) is essential- 5 years' experience in software analysis & development on I-Series (medior)- thorough knowledge of SQL and RPG ILE (free) including embedded SQL- knowledge of XML, in general and in an RPG-context- knowledge of web services/SOAP in an RPG-context- knowledge of Stored Procedures- knowledge of I-Series methods: MQ series, FTP, DDM, IFS- I-Series Software Solutions experience with RPG/400 or older- familiarity with a software change management system, preferably ALDON Lm(i)- usage of IBM Rational- Ideally you will love commutable to the offices in Brussels.
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SEC prove time and time again that they are best in class. They are responsive, go the extra mile, are passionate about what they do and show they really do care and that it isn’t just about numbers. We recently requested some market research into rates, location and compliance, and they responded to our need within the hour. They are a friend in need (no, they really are!) when help is needed.
Hiring Manager
Global CRO
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SEC have supported us with through a critical biometrics project, and have excelled in producing quality candidates throughout our partnership. They are pleasure to work with, have a supportive and attentive team, and demonstrate a keen eye for detail. I'm continually impressed with the knowledge and expertise of the SEC consultants, I trust their judgement completely.
HR Manager, EMEA
Global CRO
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We get a lot of calls from staffing agencies but what I liked about SEC’s approach was that there was not unnecessary perseverance. The team has been very sensitive about ensuring that they are in contact with us when we need them to be. The team didn't over-sell themselves and let their work speak for itself – that's what's important to us when choosing a recruitment partner.
VP, Clinical and Regulatory
Medical Device Startup, USA
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Regulatory Affairs
Sergio Carito April 2021How do I break into regulatory affairs? Trends, insights and career advice
Regulatory affairs professionals play a critical role in the pharmaceutical industry and are involved at all stages of the drug development process, providing support and direction that enables other departments involved in the process to deliver effective healthcare products across the globe. Their work ensures products are approved by pharmaceutical regulatory bodies, a vital step in bringing any new treatment to market. Why regulatory affairs?Regulatory affairs has been a cornerstone of our operations for over 20 years. There is demand for professionals at each stage of the clinical trial process, and the market is made up of a diverse range of individuals from a variety of backgrounds. The tactical and strategic industry is favoured among life scientific professionals who are looking for a career that isn’t lab-based, but is still very much on the forefront of the drug development effort. A position in the reg affairs field often brings a higher level of job security than in similar research and development positions, as product failure won’t necessarily put a regulatory affairs professional out of a job. It’s also a great route for graduates; entry-level roles are accessible for those who have a bachelors or a masters, a PhD isn’t often required.There is good career progression in within the field of RA, and once you gain experience it’s easy to move from a junior administrative role into a more senior role with advisory functions. There is also the offer of flexibility, with some senior professionals opting to freelance or provide consultative services, both options that lend itself well to working from home.What are employers looking for? A key trait for those looking to enter the field is a meticulous eye for detail. A huge requirement is analysing and submitting heavily technical documentation, which often has to be done toward a tight deadline to meet market launch dates. Organisation skills are essential, and you must be able to recognise and rectify mistakes quickly and efficiently. Communication skills are important too; Many RA professionals deal with all sorts of individuals involved at different stages of the drug development cycle, and knowing how to manage these relationships effectively is essential.The truth is that there’s no single requirement for candidates to enter the field. This makes researching roles and getting your foot in the door quite difficult and could be enough to lead a candidate to look elsewhere. Networking is invaluable for those looking to start their career, and organisations like TOPRA are great for graduates seeking career advice. An undergraduate or postgraduate scientific degree (biology, microbiology, pharmacy, biochemistry, pharmacology or similar) is the first step in getting into RA, and experience in drug development is a bonus. Candidates who are successful in the field come with a variety of backgrounds and career experiences, the only common thread being a strong interest in the drug development cycle and information analysis.The future of regulatory affairs is bright, and as with other areas within pharma, developments in artificial intelligence and machine learning mean the RA landscape is evolving. New roles are being introduced and there are new responsibilities for those in the field; There is a growing need for people to be accustomed to working with AI, and the ways in which people are working keep changing as we discover its full capabilities.It’s an exciting time to be in regulatory affairs, and demand for professionals is high. Do you have questions about your next move within the field, or seeking advice on how to begin your RA career? View our open roles or check out the specialisms page here.
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Clinical
Rebecca Law April 2021From experimental treatment to viable therapeutic: the rise of psychedelics in the treatment of mental health disorders
A mental health crisis has highlighted an urgent need for new treatment options for sufferers of anxiety, depression, and other mental disorders. This need has opened the door for a flourishing new sub-sector of the life science industry, and 2021 is set to bring new clinical research as major players tune in to the benefits of psychedelic medicines. In the US almost 1 in 5 people suffer from a mental health problem of some kind. In the UK this is as high as 1 in 4, and here reliance on antidepressants is close to double the level it was 10 years ago. The human brain, though, is complex and difficult to study, so uncovering the roots of a psychiatric illness to develop potential treatments isn’t easy. Coupled with the fact that a person’s diagnosis may change several times throughout their life, progress on developments of drug treatments for mental illness has been frustratingly slow when compared to traditional therapeutic areas. "Research and development in this area has been almost entirely dependent on the serendipitous discoveries of medications. From the get-go, none of it was ever based on an understanding of the pathophysiology of any of the illnesses involved."Thomas Insel, Former Director of the US Institute of Mental Health (NIMH)Research into the efficacy of psychedelics has boomed in the last decade as rates of mental health problems has risen and attitudes toward treatments have changed, and such research has yielded promising results. In the last two years the first treatments using drugs like psilocybin (the chemical compound present in magic mushrooms), ketamine and LSD have received approval in the US, EU and Canada, and are being ushered from the lab into pharmacies and therapists’ offices thanks to pioneering firms like COMPASS Pathways, Numinus and MindMed. Early Research and Application Following a successful $80m investment round during Q2 last year, London-based mental health care firm COMPASS Pathways is conducting a world-first large-scale trial into the use of psilocybin against treatment-resistant depression, which spans 20 trial sites in nine countries across the EU and US. The company received FDA Breakthrough Therapy designation back in 2018, and in February this year the biotech announced the expansion of its Discovery Centre as well as research collaborations with three world-leading psychedelic research scientists. "Our mission has always been to accelerate patient access to evidence-based innovation in mental health. This is more important than ever now, with COVID-19 challenging our mental resilience. This shows that our investors recognise this urgent need for innovation in mental health and will enable us to do more research and development, bringing therapies safely to those who need them, as quickly as possible."George Goldsmith, CEO and Co-founder of COMPASS PathwaysEarlier this year Swiss-based biotech MindMed announced the start of their trial measuring and evaluating MDMA and LSD, with the goal of understanding how they could be used together to create better patient outcomes and develop more advanced psychedelic therapies. It’s not the first time LSD has been used for research into mental health treatments, but it’s the first time both have been researched when used in combination with MDMA, which is hypothesised to offset some of the known negative effects of LSD that occur in clinical settings. Another major name in the field is Canadian firm Numinus, a company with an ecosystem of healthcare solutions centred around research into psychedelic-assisted treatments. At its 7000-square-foot facility, they are cultivating and harvesting the mushrooms that produce psilocybin in order to develop standardised extraction methods, research product formations of the compound, and explore the delivery of safe and evidence-based psilocybin-assisted therapies in clinics. The Future of Mental Health Care? We need more large-scale studies involving diverse populations to learn as much as we can about the way that these treatments work. There is a lot still up in the air about the effects of psychedelics to treat mental disorders, but early trials and applications are encouraging. What we do know is that psychedelic-assisted treatments can be powerful in reducing the suffering for at least some sufferers of anxiety, depression, PTSD and other mental health problems. We know that the stigma around discussion of mental health has seen a positive shift recently, so it’s a welcome sign that an increasing number of life science companies are focusing their attention on research that could lead to mental health treatments that compliment or prove more effective than those currently in the mainstream healthcare system.
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Commercial, Digital Health, MedTech
Emma Hobbs March 2021The top five stateside locations for jobs in medtech and digital health
2020 was the most funded year in history for medical technology, beating 2019 by 55% even with the pandemic, so it’s a great time to work in the medtech and digital health fields. Here are the areas that should be on your radar if you’re considering a move into the industry. Cash often dictates the top locations for medtech and digital health more than any other indicator, and more of this is being spent in fewer, more concentrated clusters across the states. These areas bring together a mix of prestigious educational institutes and strong healthcare systems, and are home to companies that bring in millions of dollars of capital investment each year. Insights from PwC suggest that this year we can expect to see the fields of robotics, wearables, genomics and diagnostics bring in a huge amount of investment and dictate M&A agreements.San Francisco, California Owing to the 3,000+ biotech and medical device firms that call it home, the area of San Francisco, San Jose and the surrounding areas of northern California is known as Biotech Bay, and has almost 100,000 life science professionals working within its borders making an average salary of $164,123. The tech sector has long been making major advances in this area, so it’s a natural hotbed for medical technology firms too. The area leads in terms of innovation with more patents filed than anywhere else in the US, and in 2019 ranked highest for VC investment in digital health, bringing in $2.7b of capital funding.New York City, New YorkBack in 2016 NYC announced a $500m deal to establish itself as a world-leader in life science R&D, and since then has cemented itself as a global leader in bioinnovation. In neighbouring New Jersey, you’ll find major corporations such as BMS, J&J and Novartis, but NYC itself has attracted a number of digital and medtech startups in recent years. New York State is now second to California when it comes to digital health VC funding. In the first half of 2020 alone $1.5b of capital investment went to the NY digital health sector, surpassing 2019 by 25%, with the largest deals among firms dealing in healthcare analytics, telemedicine and patient engagement platforms. The number of start-ups established and headquartered here creates a huge amount of opportunity for professionals, and together with New Jersey the states rank #1 for job opportunity within the US.Boston, Massachusetts A hotbed of innovation and drug development, over 600 biotech, medtech, medical device and pharmaceutical companies call Boston and its surrounding areas home. Funding levels have shown uninterrupted growth in the last decade, and total investment to companies in the city has broken the billion-dollar threshold every year since 2013, hitting a peak of $8b in 2019. Among this list Massachusetts is the only state that showed a significant increase in the amount of VC funding to digital health firms from 2018 to 2019, with a 37% increase from $704m to $1,033m. High-calibre universities and local research institutions like Harvard, MIT and Tufts provide the city with a strong pipeline of future innovators. It’s estimated over 700,000 professionals with backgrounds in biology, biomedical sciences and engineering reside in Boston and its surrounding counties.San Diego, California With California housing 10% of the worlds’ top 100 universities, it’s unsurprising that it isn’t just northern California making its mark on the digital health and medical technology industry. Southern California, specifically San Diego but also LA and Orange County, is home to around 1,400 health technology firms. The average wage is a little lower than upstate, coming in at $127,345, but opportunity is rife with the industry employing more than 140,000 people.Raleigh-Durham, North Carolina Anchored by three major universities, North Carolina State, Duke and University of North Carolina, is the region referred to as the Research Triangle. More than 500 life science firms operate in the area, and thanks to the formation of IQVIA the area is known as the birthplace of the CRO. But CROs and multinationals aren’t the only companies booming in Research Triangle; cutting-edge cell therapy companies and ground-breaking medical technology firms are examples of the type of companies that have established themselves in the area over the last decade. Innovation, education and a culture of collaboration are key drivers of the area’s success, and we can expect it become increasingly associated with cutting-edge medical technology in the coming years.Seeking your next move? Check out our latest jobs here.
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TeamSEC
Louis Gicquel March 2021We’re elevating the offering we provide to our life science partners – here’s how
Equipped with almost 40 years combined experience in life science recruitment, our new Client Services division offer a bespoke approach to staffing by responding to your business goals and unique pain points.For over 30 years we have been building companies in the global life sciences industry. From start-up and emerging biotechs to global pharma, innovative medtech and medical device companies to strategy and tech transformation consultancies; we deliver talent solutions that enable our clients to achieve their mission.It’s our ongoing commitment to providing a well-rounded and bespoke staffing solution that has led to the appointment of a dedicated Client Services Division within SEC. The Client Services team work with our partners to develop and deliver a growth strategy that’s tailored to the goals of each business. Working with our partners to gain an in-depth understanding of the organisation, the team are able to provide strategic direction when it comes to headcount and team structure, and develop an approach that ensures the best possible chance of reaching that next company milestone, whether it be a trial launch, product commercialisation, funding round or major buy-out.The division is complemented by a team of market experts focused on providing recruitment services across a variety of specialisms; discovery & development, clinical & medical, data science, machine learning, artificial intelligence & biometrics, tech ops, strategy and commercial. We've been providing services in these areas for years, and look to continually develop our expertise with the changing life sciences landscape.Our Client Services TeamLouis Gicquel, Client Services DirectorLouis brings over 15 years of life science staffing experience to our client services division, and has provided leadership as our sales director at SEC since 2017.Emma Hobbs, Client Services ManagerWith more than 11 years experience supporting SEC clients and a further 5 in staffing and recruitment, Emma heads up our operations in the US and provides solutions to our clients in the medtech, biotech and consultancy space.Rachael Conroy, Principal ConsultantRachael has 5 years of life science staffing and account management experience, and is responsible for providing services within the DACH region.Our Client Services ProcessStage 1: AttractWe'll conduct a deep dive into the purpose, goals and fabric of your business to uncover opportunities for growth and the structural and headcount changes you might need to make to achieve them.Stage 2: AssessWe'll devise and present a fully bespoke recruitment program utilising all our routes to market, presenting you with the most relevant, qualified and motivated candidates.Stage 3: AttainWe'll work on collaborative campaigns to support you in telling the story of your business. we’ll provide updates on the candidate market, work with you on employer branding campaigns, and engage passive candidates on your behalf so you're always ready when it comes to hiring.We’re delighted to be able to service more of our partners’ needs through continual development of our solutions. Appointing a dedicated Client Services function ensures that we continue to deliver best in class service, at speed, to support the growth of our clients across the life sciences space. To understand more about how we can support your growth and provide strategic input tailored to your business, get in touch today.
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Biometrics, Big Data, Artificial Intelligence
Wayne Marshall March 2021Machine learning: The next frontier of drug discovery and diagnosis
The drug development path is long, complicated, and expensive. For the patients that need it most, waiting for a treatment can be agonising, and currently 95% of rare diseases lack any FDA-approved treatment. Artificial intelligence and its subfield of machine learning has the power to change this.Approval rate for drugs entering clinical development is less than 12%, and with the average cost of developing a prescription treatment sitting at $2.6 billion, those in drug development are turning to technology that detects signs that might indicate a greater likelihood of product success or approval, whilst the product is still in the discovery or R&D phase. It can take over 10 years from discovery to commercialisation of a treatment, so a huge motivator for large pharma to invest in this type of technology is the potential to shave time from this process. An oncology programme from Genentech (now a member of the Roche Group) and GNS Healthcare announced back in 2017 uses machine learning tech to covert high volumes of cancer patient data into computer models that can be used to identify new pathways, novel targets and diagnostic markers that could lead to new treatments. The benefits of utilising artificial intelligence reach far beyond just a cost or time saver for the company developing the drug. Synchronicity of real-world data and machine learning technology can shorten the amount of time it takes for a patient to receive a diagnosis and reduce the likelihood of a misdiagnosis. In medical diagnosis a patient’s symptoms are recorded, analysed, and a healthcare professional aims to determine the ailment that could be causing them. Machine learning technology can take a set of data – consisting of clinical or biological criterion of patients, any diagnoses they’ve received, and any environmental and genetic data – and match these with the data collected from a patient. The larger the data set, the more points of reference the AI will have to determine a diagnosis, and the greater the likelihood of an accurate one. One example of a firm currently using machine learning to aid diagnosis is UK-based start-up Babylon Health. Their chatbot technology compares the symptoms inputted by a user against a database of potential causes, and recommends an action based on the symptom severity, the history of the patient and other individual circumstances. In response to mild headache symptoms, the app may recommend over-the-counter medication, but if more serious symptoms are inputted, the app may suggest going directly to the hospital. This does present a limitation in that the performance and accuracy of the technology is dependent on the depth of the dataset, but it’s a promising indicator that these processes could take place without the need for human intervention, meaning patients get quicker access to the care and information they need. Machine learning is becoming more widespread, is attracting a huge amount of media attention and capital investments, and outcomes are becoming increasingly impressive. There is still a distance to cover, though, before it really hits the mainstream. Before cementing itself as a standard component in the drug development cycle, educational programmes, thorough proof-of-concept studies and data hygiene standards have to be considered. Until then, these early applications of machine learning in medicine provide glimmers of a future where data and technical innovation play a critical role in discovery and development.
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Biometrics, Clinical, Big Data
Catalin Zaharia February 2021What is real-world data, and how can it be used to inform healthcare strategy?
We are living in the age of big data. Drug development companies are swimming in information that can inform their processes and assist them in bringing a treatment to market; but this information is no longer solely generated through clinical trials.As the cost of healthcare continues to rise and companies face pricing pressures, there comes a growing need to demonstrate the benefits of a treatment outside the regulated environment of a clinical trial. So, companies are turning to real-world data (RWD) to demonstrate the value of their product on a real-world population.What is real-world data? Any insights into a treatment gathered outside of a clinical trial setting could be a source of RWD. Health records, wearable devices, healthcare apps, patient-recorded outcomes, even insurance claims all can provide evidence to support the effectiveness of a product. As it’s captured within the healthcare system itself, against real patients rather than trial subjects, it can provide an additional dimension to observations gathered during clinical trials. Why is real-world data so important? With a deeper insight into how treatments are being used and the effects of a drug, RWD can provide regulators the information they need to assess post-market safety and produce risk/benefit analysis; key enablers for regulatory decisions and market approvals. The data can not only inform decisions made regarding commercialisation, but can help inform those involved in research and development as to the needs and requirements of a patient population. But the scale of data available does far more than help companies bring their treatments to market quicker. Importantly, it enables us to further understand the patient journey, and provides a huge opportunity for companies to improve patient outcomes. By producing RWD, patients act as integral participants in the future of their own healthcare. What does the future of real-world data look like? The sheer amount of data currently available is overwhelming; for one treatment there could be hundreds of thousands of seemingly relevant pieces of RWD, and most organisations lack the resources to effectively collect and analyse it, which is why we’re seeing larger firms invest in machine learning technology or partner with start-ups specialised in AI. We’re also seeing a rise in demand for professionals with RWD/RWE experience. Some of the larger industry players will follow in the footsteps of companies like IQVIA, in establishing and developing their own RWD capabilities and offering. We’ll see more cross-departmental collaboration, among physicians, pharmacists, statisticians and pharmacologists, as we work to discover new ways of collecting and analysing RWD. Advances in cloud-based technology, artificial intelligence, and automation could help smaller firms discover the benefits of using RWD. Providing them with more access to information about who their treatments effect, in what context, and at what price, will shorten their product pipeline and enable faster patient access. Ultimately, continued data openness will enable companies to develop forward-thinking healthcare strategies, such as personalised medicine, which can address previously unseen problems and put the patient population at the heart of treatment production. As machine learning technology also advances, we’ll see healthcare professionals be able to make faster, more accurate diagnoses through access to this real-world data, and variables that might’ve been previously overlooked will be used to inform a deeper understanding of patients’ conditions.
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Clinical
Jacob Stafford-Wright February 2021Women in Science Day 2021: Four life science pioneers shaping modern medicine
February 11th marks International Day of Women and Girls in Science, a day that recognises and celebrates the critical role women play in STEM industries. Since 2015 the number of women graduating in core STEM subjects in the UK has grown from 22,000 to almost 25,000, but still females make up only 26% of those graduating in STEM subjects, and just 24% of the average STEM workforce – this figure drops to as low as 10% for some industries. Now in its sixth year, the International Day of Women and Girls in Science was adopted to pave the way toward gender parity in educational opportunity within STEM and scientific participation and preparation. To celebrate this year, we’re looking at four pioneers within the life science industry that are transforming the medical landscape through leadership and technical innovation.Carolyn Yarina, CEO and Co-Founder of Sisu Global HealthWhen a patient suffers internal bleeding, surgeons have two options; reach for a blood bag, or recycle the patient’s own blood using a process called autotransfusion. In many developing countries, though, lack of access to blood banks or a lack of blood donorship might mean the surgeon doesn’t have access to a blood bag, and the technology typically used for autotransfusion is expensive and requires power – a commodity not always available in emerging markets. After founding a non-profit that supported mobile clinics in India, Carolyn went on to co-found Sisu Global Health, a company focused on the research, development and commercialisation of medical devices aimed at emerging markets. The Sisu-developed Hemafuse, a handheld medical device that replaces the need for donor blood by recycling a person’s own from internal bleeding, launched in Ethiopia, Kenya and Ghana last year. Allysa Dittmar, President and Co-Founder of ClearMask With over 95% of those living with hearing loss saying masks and facial coverings impact their ability to communicate, Allysa, who has been deaf herself since birth, set out to design a transparent mask with her fellow public health students at Johns Hopkins University and co-founded ClearMask LLC. Allysa and the team at ClearMask have developed the first FDA-approved transparent face mask, allowing for the deaf and hard of hearing that would usually rely on lipreading for communication to do so clearly, without the obstruction a standard face mask would cause.Dr. Crystal Icenhour, PhD, CEO and Co-Founder of Aperiomics A rising star of American biotechnology, Dr. Crystal Icenhour holds two patents, has authored and co-authored numerous scientific publications and is a prolific speaker at many scientific conferences. In 2014 she co-founded Aperiomics, a bioinformatics firm that uses advanced data analysis and next-generation sequencing technology for detecting infectious disease. Where traditional infection testing might look at one bacteria, fungus or virus at a time, DNA sequencing technology developed by Dr. Crystal’s firm can identify every known pathogen there is – that’s nearly 40,000 microorganisms – from within a single blood sample. It’s the mission of the infectious disease firm to transform infection testing, and leverage the power of technology to advance human life and quality of life. Dr. Kimberly Smith, MD, MPH, Head of R&D at ViiV Healthcare Dr. Kimberly Smith heads up research and development at the only company wholly dedicated to HIV therapies, ViiV Healthcare. During her time at ViiV Dr. Kimberly has launched more than 25 late-stage trials for seven new medicines, and is working to revolutionise the management of HIV through regimes that decrease the lifetime exposure to medicines by suffers of HIV. Since working on the frontline of the AIDS epidemic as a clinician in the 1980s, Dr. Kimberly has made it her life work to answer the unmet needs of those living with the illness, and has been a public advocate for female and PoC representation in STEM professions and in exec level roles.
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Clinical
Reece Harding February 2021When it comes to demand in the clinical sector, Covid-19 remains top priority
More than a year has passed since Covid-19 first hit the headlines, and across the world nine vaccines have received authorisation for use in various geographies. But for firms involved in researching and trialling treatments for the virus, it isn’t job-done just yet. When it was announced that some of the major frontrunners in the race to develop a Covid-19 had succeeded in their mission, a collective sense of relief was felt, and the eyes of the public shifted from trial progress to the vaccine roll-out. But for those working in the clinical space, the priority remains with the effort to develop further treatments. With over 2,500 clinical trials in active or recruiting stage globally, opportunities for professionals in the clinical operations field are still dominated by the Covid-19 effort – particularly when it comes to the contract/freelance market.Mutated strains of the Covid-19 virus pose a potential new threat to the geographies in which they’re circulating, adding weight to the burden already felt as a result of the pandemic. These mutations emphasise the importance of the result of these ongoing trials, almost 75% of which are in phase II or phase III stage, as researchers continue to uncover the indirect or long-term effects suffered by those who have had the virus. With the US, Germany and the UK all topping the list for the highest number of ongoing vaccine studies, demand for CRAs, clinical trial managers, and site managers is high to cope with the demand on the major trial sites in those geographies. Shortly after the World Health Organisation first declared Covid-19 a global emergency and much of the world entered a lockdown, many ongoing and new clinical trials were halted to prioritise studies into the virus and continued later in the year. The ripple caused by the halting of these trials, along with the fact new Covid-19 vaccine trials are registered to begin each week, suggests that this high level of demand for clinical professionals will continue throughout 2021 and well into 2022. The length of Covid-19 trials being registered are also longer on average than we saw at the beginning of the pandemic, so we can expect the average contract length for freelancers to increase too.We can expect to see more vaccines demonstrating high efficacy in the coming months, as well as a deeper understanding of the long-term effects of Covid-19 and how to treat them or stop them from occurring. The current vaccine roll-out effort continues to progress and make headlines, but in order to advance our knowledge of the virus and its variants, clinical trials and research into treatments or preventative measures for Covid-19 will continue to progress at a high level too.
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TeamSEC
Jacob Stafford-Wright January 2021SEC Hits Recruiter's Hot 100 List for 2020
SEC Recruitment has been announced as one of Recruiter Magazine’s ‘Hot 100’ companies in the UK for 2020. The accolade is based on ranking recruitment businesses for their productivity, which is a key performance indicator used to assess businesses that are working at high levels across the recruitment industry. "We’re truly proud of our approach to the difficulties faced in 2020 and the support we've been able to provide our partners - some of whom were at the forefront of the efforts against Covid-19 themselves. The work our team has put into delivering the best possible service to our clients and candidates throughout the last 12 months is both brilliant and humbling."Wayne Marshall, Sales Director at SEC RecruitmentIt's been a truly disruptive year for the staffing industry as a whole. Analysis from this years' report suggests an unsurprising dip in performance compared to previous years, so we're especially pleased to be recognised for our performance and proud of the incredible work put in by our recruitment consultants and back-office support team.SEC comes in at number 90 this year, and is one of just 24 technical/science recruitment specialists to appear on the list, which looks at the performance of over 15,000 staffing agencies up and down the country."We're delighted that we have been included in the ‘Hot 100’ list for 2020. This year has proven that when you work hard and deliver on your company values and commitment to excellence, you can continue to deliver results even in the most adverse of climates."Louis Gicquel, Sales Director at SEC RecruitmentThanks go out to all of our customers that we have worked with throughout 2020, and to the candidates we've supported in finding their next role. We're looking forward to continuing to play a part in your success in 2021.For more information about the ‘Hot 100’ visit the Recruiter website.
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Wayne Marshall January 2021
How can your business maintain a flow of freelance and contract talent?
In a time when engaging freelance talent is becoming increasingly attractive, does your business have a strategy when it comes to engaging contractors and maintaining a relationship?Being clued up on legislation to follow when you’re engaging freelance talent is one thing (such as the looming IR35 update, if you’re in the UK), but with contract employment on the rise in the wake of a new normal the competition when it comes to engaging talent is fierce; 79% of employers that we surveyed said they were employing the same amount or more contractors this year than they had in previous years. So with more and more businesses utilising the benefits of a freelance workforce, contract workers once competing for jobs now have multiple options when it comes to projects, and may find themselves able to cherry-pick their client pool. Therefore, it’s never been more important to introduce a process for engaging and building a relationship with your off-payroll workforce. Employer Poll: "How will the number of contractors/freelancers you work with in 2021 differ from in previous years?"Engaging contractors should look different to how you engage your employees. You should look to position yourself as a company of choice when seeking to work with freelance talent, but it’s important to remember not to treat them as an extension of your permanent workforce. For UK businesses, freelancers engaged in projects that fall outside IR35 should be handled as a business-to-business agreement. Understand that positioning yourself as a business of choice when it comes to contracting opportunities is more about your business objectives, milestones, and successes than it is about what it’s like to work for you as an employer. Your contractors don’t want to feel as though they are being treated like an employee, and failure to recognise this could affect your flow of off-payroll talent through word-of-mouth amongst disgruntled freelancers. Turn to a staffing firm for full-circle contractor care. Staffing companies can provide a crucial insight into how and where to get the best contract talent for your projects, but many businesses without the internal resource or know-how also turn to agencies to maintain a relationship with their contractor base even after a project has ended. Freelancers turn to agencies to understand the latest developments and opportunities in the industry, and trust us to provide an honest view of the contract landscape. Having these conversations every day means we’re not just in a great position to engage talent for a particular project, but to enhance our clients’ reputations on their behalf and keep their work at the forefront of the minds of leading talent. We are aware of many countries looking to challenge the statuses of independent contractors, but with over 200 contractors on-site globally, our in-house compliance team are versed in local regulations of major employment sites across Europe, the US and further afield, and are committed to ensuring compliance on behalf of our contractors and clients. Get in touch to find out more about our compliance offering.As workforces continue to become more mobile, more adaptable and more collaborative, contract talent will become increasingly embedded in business strategy. Those already engaging contractors have the chance to get ahead of the curve and strengthen the relationship with their contractor base, and those new to engaging freelancers have an opportunity to hit the ground running knowing the importance of contractor care.
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