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Location (East) within 20 miles; Sector: Biotech / Pharmaceuticals; Posted within: 8 weeks
 
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  • You’ll work well alongside the DMO Team Manager to ensure all tasks documented in the sponsor contract are completed on time and monitor project budge...
  • This is an important position, managing all the regulatory activities and packages that apply to our clinical work across a range of countries. You wi...
  • The successful candidate will have four to six years’ experience in a CRO, pharmaceutical or finance/operations environment and at least a year as a d...
  • The successful candidate will be PMP qualified or have equivalent professional experience, preferably in a pharmaceutical organisation or CRO. A backg...
  • We are looking for a senior regulatory specialist to co-ordinate our clinical trial and marketing authorisations and develop regulatory packages for e...
  • The successful candidate will have several years’ experience in a similar position - preferably in the pharmaceutical industry - three years’ involvem...
  • 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. ...
  • With a considerable track record of leading a specialist sales team, you will have substantial experience of implementing and leading a KAM framework....
  • 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...
  • 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. ...
  • 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. ...
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