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Salary: £70,000
Date Posted: Friday, 20th of May 2011
Description
Senior Medical Advisor
Surrey
Permanent £70K plus car allowance and bonus
Join this dynamic global pharmaceutical leader to provide medical knowledge in support of one marketed brand and one or more developmental compounds.
Responsibilities:
· Development of strategy and key marketing messages
· Development of promotional copy
· Input…
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Salary: Negotiable
Discipline: Clinical Operations
Date Posted: Wednesday, 18th of May 2011
Description
Clinical Project Director
London
Interim - 6 months initially
We are looking for Project Director level candidates, who are clinical development scientists that are also comfortable with operations (all of our studies will be outsourced). You will need to be able to function in the dual role and lead at…more info »
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Salary: Negotiable
Date Posted: Monday, 16th of May 2011
Description
EU Regulatory Strategist
This is a 6 month contract role based in Surrey.
Reports to: EU Regulatory Strategy Portfolio Manager.
Your role:
- Will be to ensure EU contribution to Global Regulatory Strategies and implementation plans.
- Ensure that the regulatory contributions work towards…
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Salary: Extremely Competitive
Discipline: Clinical Operations
Date Posted: Friday, 13th of May 2011
Description
This is an excellent opportunity for someone with exceptional clinical and medical expertise to drive the development of our client's innovative new therapies in Rheumatoid Arthritis. Your role will be imperative and high profile with a global focus, as you take responsibility for all aspects of at least one international…more info »
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Salary: High Daily Rates
Date Posted: Friday, 13th of May 2011
Description
6 month Interim contract
High Daily Rates
A rare interim opportunity has arisen for an experienced interim Medical professional to join a top 10 global pharmaceutical company.
Responsibilities may include:
· Provide dermatological medical and scientific expertise and opinion to support EU commercial colleagues and medical colleagues in European operating…more info »
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Salary: Negotiable
Discipline: Regulatory Affairs
Date Posted: Thursday, 12th of May 2011
Description
Regulatory Affairs Consultant - CMC
This is a 6 month contract role based in Maidenhead. You will be responsible for managing life cycle submissions and providing submission strategy for all registration activities with the required markets.
Main responsibilities:
Provide submission strategy for execution of lifecycle submissions associated to…more info »
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Salary: £33.00 per hour
Discipline: Data Management
Date Posted: Friday, 6th of May 2011
Description
Clinical Data Analyst required to work on contract for a Blue-Chip Pharmaceutical organisation in the South-East, UK.
Main duties of the role includes:
* Perform CRF/eCRF data validation to ensure data integrity and quality.
* Issuing data queries (DQs) manual or automated and maintenance of CRF according to DQ replies…more info »
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Salary: Negotiable
Discipline: Data Management
Date Posted: Thursday, 5th of May 2011
Description
Contract Project Data Manager required to work for a leading Pharmaceutical organisation in the South-East, UK.
Key responsibilities for the position are as follows:
· Provides data management expertise and direction to the Project Management Team
· Provides input to the Project Management Team to define the data flow timelines,…more info »
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Salary: £70,000 - £75,000
Date Posted: Wednesday, 4th of May 2011
Description
EU Medical Advisor - Neuro
Hertfordshire
Salary negotiable
Role:
Provide medical affairs support for pre and post launch activities for existing and future products for Northern Europe
Provide medical affairs support for local market access activities in Europe North Region
Align with Europe North Medical Director for key governance requirements…more info »
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Salary: £50,000
Discipline: Data Management
Date Posted: Wednesday, 4th of May 2011
Description
Senior Data Manager required to work for a leading Pharmaceutical organisation in Germany whereby you will be responsible for:
Preparing, conducting and closing of data management activities (such as design of Case Report Forms (eCRFs), patient diarys (ePRO), Data Management Plan, database structure and consistency check specifications, data review, SAE…more info »
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