SEC Pharma
+44(0)20 7255 6600
+33 (0)17 0807 489
+49 (0)69 2222 2888
+41 (0)44 5803 717

quick job search

All Permanent Contract

advanced job search

All Permanent Contract

all job categories
Biometrics
Clinical Research & Development
Drug Safety & Pharmacovigilance
Healthcare & Hospitals
HEOR & Market Access
Medical Affairs & Communications
Pharma IT
Pharma IT
<< Back
    Currently we are not recruiting for any roles in this category.
    QA & QC
    Regulatory Affairs
    Sales, Business Development & Marketing
    Scientific, Engineering & Manufacturing
    search results
    Below are a list of jobs that match your search criteria.

    Senior Clinical Project Lead

    I am happy that my client, a successful pharmaceutical company has opened a new position as Senior Clinical Project Leader. The position offers you a strategic part, line management, vendor management and budget responsibility. An innovative and leading pharmaceutical company is now looking for an international Senior Clinical Project Lead in Southern Germany, office based.

    Not Specified
    Germany

    Associate Director Site Contract Management Germany or Austria

    Associate Director, Site Contract Management Germany or Austria A massively expanding global CRO with an excellent reputation on the market and strong pipeline of new projects is seeking an Associate Director specializing in Contract Management to join their organisation on a permanent basis. – Very competitive salary and remuneration package – home based possibility –

    Not Specified
    Germany

    Lead/Senior SAS Programmer – SWITZERLAND Office

    SEC/JLP/SAS/SW/220515
    Lead/Senior SAS Programmer – SWITZERLAND Office
    Very competitive salary + Amazing Benefits Package
    PERMANENT ROLE

    My client in SWITZELAND is now looking for a Lead/Senior SAS Programmer. By working on innovative projects in the pharmaceutical environment, you will be involved in a new and challenging project while developing your skills and your career. This is an amazing opportunity!

    As a Senior/Lead SAS Programmer, you will be in charge of:

    *Ensure that projects are well documented
    *Be involved in leading project, meet deadlines and deliver high quality work
    *Contribution to the SAS project management (implementation of strategic solutions)
    *Interaction with statisticians regarding frequent requirements
    *Responsible for all tasks related to the statistical programming: Production of TFL, creating macros…
    *Communication with the project team members
    *Production of statistical annexes with proper documentation

    To succeed in this role, you will have the following skills and profile:

    *Master in Science and Statistics, Computer Science or a relevant field is desirable.
    *Demonstrated professional experience as a Senior SAS Programmer, developed in a pharmaceutical company, CRO or Biotech / Biopharma
    *Demonstrated experience in creating macro, TFL production and all tasks related to the statistical programming
    *Experience in CDISC data standards (SDTM, ADaM)
    *Understanding of database structures and complex data structures
    *Excellent communication and presentation of results skills
    *Ability to meet strict deadlines and to work as part of a team

    To send your application, please contact:

    Jonathan Perruque
    Consultant – Pharmaceutical, Healthcare & CRO Division
    Statistics, Biostatistics & Programming
    Tel: +44 (0) 207 255 66 65
    jonathan.perruque@secpharma.com
    uk.linkedin.com/in/jonathanperruque/en

    Excellent Salary + Amazing Benefits package
    Switzerland

    Lead/Senior SAS Programmer – SWITZERLAND Office

    SEC/JLP/SAS/SW/220515
    Lead/Senior SAS Programmer – SWITZERLAND Office
    Very competitive salary + Amazing Benefits Package
    PERMANENT ROLE

    My client in SWITZELAND is now looking for a Lead/Senior SAS Programmer. By working on innovative projects in the pharmaceutical environment, you will be involved in a new and challenging project while developing your skills and your career. This is an amazing opportunity!

    As a Senior/Lead SAS Programmer, you will be in charge of:

    *Ensure that projects are well documented
    *Be involved in leading project, meet deadlines and deliver high quality work
    *Contribution to the SAS project management (implementation of strategic solutions)
    *Interaction with statisticians regarding frequent requirements
    *Responsible for all tasks related to the statistical programming: Production of TFL, creating macros…
    *Communication with the project team members
    *Production of statistical annexes with proper documentation

    To succeed in this role, you will have the following skills and profile:

    *Master in Science and Statistics, Computer Science or a relevant field is desirable.
    *Demonstrated professional experience as a Senior SAS Programmer, developed in a pharmaceutical company, CRO or Biotech / Biopharma
    *Demonstrated experience in creating macro, TFL production and all tasks related to the statistical programming
    *Experience in CDISC data standards (SDTM, ADaM)
    *Understanding of database structures and complex data structures
    *Excellent communication and presentation of results skills
    *Ability to meet strict deadlines and to work as part of a team

    To send your application, please contact:

    Jonathan Perruque
    Consultant – Pharmaceutical, Healthcare & CRO Division
    Statistics, Biostatistics & Programming
    Tel: +44 (0) 207 255 66 65
    jonathan.perruque@secpharma.com
    uk.linkedin.com/in/jonathanperruque/en

    Excellent Salary + Amazing Benefits package
    Switzerland

    Contract Senior Medical Writer – 6 months – UK Home based – Glo

    I’ve very recently been instructed on a 6 month Medical Writing contract with a Global CRO. It’s a home-based position in the UK and they are looking for someone with prior experience as a Senior Medical Writer within a Pharma or CRO. As SMW your role will involve the development and delivery of Clinical and Regulatory documents including Clinical Study Reports (CSR) and Clinical Protocols.

    For more details please call me on 0207 255 6665

    Not Specified
    England

    Senior CRA – Oncology

    Senior Clinical Research Associate – Oncology Home Based Anywhere in UK or Ireland Roles outsourced to Pharmaceutical Companies also available A leading CRO with an extensive portfolio of clients, including exclusive agreements with high-profile sponsors is seeking a CRA II or Senior CRA with strong experience in Oncology, to monitor projects predominantly within this therapeutic

    €48000 - €60000 per annum + Car/Allowance, Annual Bonus & Benefits
    England

    Senior Director, Alliance & Project Management – Late Phase

    Senior Director, Alliance & Project Management – Late Phase Home Based, or Office Based in West London A multi-national CRO with an impressive portfolio of clients is currently seeking an experienced individual for the position of Senior Director, Alliance & Project Management – Late Phase on a permanent basis. The role-holder will be able to

    £80000 - £100000 per annum + Negotiable
    England

    Clinical Project Manager (Full-Service)

    (Senior) Clinical Project Manager Home Based, Anywhere in UK or Office Based in Greater London An international Contract Research Organisation with strong growth plans and a proven history of delivering clinical trials for major sponsors is currently seeking a Clinical Project Manager with at least 18 months experience for a new role within their project

    £50000 - £65000 per annum + Negotiable Salary, Strong Benefits Package
    England

    Clinical Research Associate II – Ireland

    Clinical Research Associate II Home Based Anywhere in Ireland or Office Based in Dublin A leading international CRO currently enjoying record revenues is seeking experienced CRA’s to join their growing clinical operations team in Ireland on a permanent basis. Please note that in addition to seeking candidates at CRA II level, the business is seeking

    Not Specified
    Republic of Ireland