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Location (Welwyn Garden City, Hertfordshire) within 20 miles; Sector: Biotech / Pharmaceuticals; Posted within: 8 weeks
 
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  • As Clinical Programmer you will be involved in supporting global data handling activities by providing study databases and reporting tools for clinica...
  • The UK Clinical Projects Group, within the Medical Affairs Department is a rapidly evolving team of Project Managers and Clinical Trials Assistants de...
  • We are recruiting for the position of Senior Quality Rick Specialist to join our international team. Reporting to the Principle Team Lead for Service...
  • You will apply your extensive experience in pre-launch marketing to maximise the potential value of a variety of pipeline products. You would be the ...
  • To further strengthen our national Regulatory Affairs group, part of the Medical Department, we have an exciting opportunity for an experienced regula...
  • You’ll draw on your experience of multiple sclerosis as you work to develop market insight to shape positioning and develop pre-launch brand strategie...
  • A new opportunity has arisen to join the Clinical Data Management team. We are recruiting for a Study Data Manager to take the lead for the planning a...
  • As a member of the Marketing Insight and Analysis Group (MIAG) you will make an important contribution to the successful marketing and selling of the ...
  • Here is an exciting opportunity within our Quality Department. We are recruiting for Principal Systems Validation Analyst to provide expertise in supp...
  • You will be responsible for the production of non-CRF data collection, specification, documentation and for defining the study specific non-CRF data h...
  • • Exposure to cultures and business practices of different countries; opportunity to identify GSK global best practices. ...
  • Develop and implement the product safety strategy and overall risk/benefit assessment, Integrate, analyse and clinically interpret safety information...
  • The role will require you to be medically qualified having obtained a medical degree or PhD along with a minimum of 7 years progressive experience in ...
  • Clinical Data Manager
    Biotech / Pharmaceuticals
  • Cmed (Clinical Research Services) Ltd
  • United Kingdom
  • 02/05/12
  • You will have strong organisation and communication skills and a thorough understanding of medical terminology, physiology, pharmacology and the drug ...
  • Responsibilities include improvement and development of operational and financial processes, management of our central information system and regular ...
  • In this role you will be able to work from one of our offices or work from home. A large part of Covance employees are able to have the flexibilty to ...
  • In this role you will be able to work from one of our offices or work from home. A large part of Covance employees are able to have the flexibilty to ...
  • The primary activity of the SAS Programmer is to develop and review SAS® programs and output for the management and reporting of clinical trial data. ...
  • In this role you will be able to work from one of our offices or work from home. A large part of Covance employees are able to have the flexibilty to ...
  • You will have at least two years experience in a CRO, pharma/biotech outsourcing or software company in a similar role. A Bachelors degree in a busine...
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