SEC Pharma
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Below are a list of jobs that match your search criteria.

Pharmacovigilance Executive

My client are a global full service CRO with offices in Berkshire. They require a Pharmacovigilance Executive to join them on an 18 month contract to act as maternity cover. This is a fixed term contract with an annual salary and company benefits. Job Summary  Supports pharmacovigilance activities.  Sets up safety databases. 

Not Specified
Slough, England

Associate Director Clinical Operations

Eine kleine aber gut etablierte CRO sucht gerade einen Associate Director Clinical Operations für seinen Headquarter in Deutschland. Diese CRO, die auf dem gesamten europäischen Markt operiert möchte nun einen besonders starken Fokus auf den deutschen Markt legen. – Festanstellung – wettbewerbsorientiertes Gehalt – homebased oder office based – unbefristete Vollzeitstelle Sie bekommen hier die

Not Specified

Junior SAS Programmer – UK Office

Junior SAS Programmer – UK Office
Very Competitive Salary + Benefits package

Amazing opportunity for a Junior SAS Programmer with experience within the Pharmaceutical industry. A global organization is now looking for an experimented Junior SAS Programmer to join their team. This opportunity will give you the chance to use your skills for the benefit of an international company, be involved on innovative projects as well as having an exceptional career progression plan.

As a Junior SAS Programmer, you will be in charge of:

*Responsible for all tasks related to the statistical programming: Production of TFL, creating macros…
*Produce and maintain the technical database standards as well as Programming Specification documents
*Contribution to the SAS project
*Be involved in new project, meet deadlines and deliver high quality work
*Contribution to the development and maintenance of applications used for analysis and reporting purposes.
*Interaction with project managers and sponsors on all aspects of programming.

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

*BSc in Science and Statistics, Computer Science or a relevant field is desirable.
*Demonstrated professional experience as a Junior SAS Programmer, developed in a pharmaceutical company, CRO or Biotech / Biopharma
*Demonstrated experience with macro, TFL production and all tasks related to the statistical programming
*Knowledge of statistical computing applications (SDTM / ADaM, Base SAS, SAS/STAT and SAS Macro)
*Ability to meet strict deadlines and to work as part of a team
*Understanding of database structures and complex data structures
*Good organizational, interpersonal and communication skills

By joining the company you will receive:

*A training panel for your profile and supported by the company
*A pleasant and innovative working environment in an international and multicultural context
*An individual career development plan that encourages long term growth within the company

To send your application, please contact:

Jonathan Perruque
Consultant – Pharmaceutical, Healthcare & CRO Division
Statistics, Biostatistics & Programming
Tel: +44 (0) 207 255 66 65

Excellent Salary + Benefits package

Senior Manager, Global Regulatory Affairs MEA

SEC is currently collaborating with a major global generics company (part of a bigger healthcare group) whose affordable medicines are currently available to 90% of the world’s population. I have personally been tasked with find an inovative, stategic thinking regulatory professional to join their Global Regulatory Affairs Department within the MEA team at Senior Manager

€80000 per annum + bonus, benefits, relocation
Bavaria, Germany

CRA II und Senior CRA

CRA in Deutschland gesucht für eine euopäische aufstrebende CRO mit deutschem Headquarter Eine kleine aber gut etablierte CRO sucht gerade einen CRA für seinen Headquarter in Deutschland. Diese CRO, die auf dem gesamten europäischen Markt operiert möchte nun einen besonders starken Fokus auf den deutschen Markt legen. – Festanstellung – wettbewerbsorientiertes Gehalt – homebased –

Not Specified

Regulatory Affairs Manager (home-based)

A global pharmaceutical company is looking for a Regulatory Affairs Manager in the South East. The purpose of this role will have to deliver and maintain competitive licences for European commercial brands. The ideal contractor will ensure timely submission and approvals of all licensing applications and compliance with European regulatory requirements. The ideal candidate would

Not Specified
South East England, England

CMC Regulatory affairs consultant – home-based

A pharmaceutical company is looking for CMC Regulatory affairs consultant – home-based. Missions: *Guide the Global RA-CMC group as a member of senior staff *Envisage the pharmaceutical industry environment and prepare for the future risks from RA perspective *Lead the preparation of submission documents (Module 3 for MAA or license variations and respond to questions

Not Specified
Hertfordshire, England


Global Studies Manager My client, a Global Pharmaceutical Company is now looking for an independent, driven individual to join its team at Global Study Manager level, on an initial 12 month contract in Welwyn, Garden City. Responsibilities: � Performs ongoing vendor management (e.g., CROs, Central Labs, IVRS, Reading Centers), including independent negotiation of scope of

£300.00 - £400.00 per day
Welwyn Garden City, England

Snr. statistician required for fun and friendly biometrics team

The consumer health care arm of a global pharmaceutical company in the south east is urgently seeking a talented statistician to join their fun and friendly biometrics department on a 12 months contract. The successful candidate can expect to be providing expert statistical advice and process oversight for all responsible projects.

£400 - £455 per day
South East England, England

Midweight Medical Copywriter – South East, UK

I’m looking for a Midweight Medical Copywriter in the South East, interested in joining a creative and bespoke independent agency. Developing copy and concepts for pharmaceutical and healthcare clients. Operating in a key role within the agency you’ll have the opportunity to work across their impressive client portfolio and build upon your experience.

For a confidential consultation call Tim Moody on 0044 (0) 207 255 6665 or email your CV to

Not Specified
Buckinghamshire, England