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Location (Hampshire) within 20 miles; Sector: Biotech / Pharmaceuticals; Posted within: 8 weeks
 
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  • To be an expert on the ABPI code of practice and to ensure and monitor company compliance with the codes and other company policies, Be responsible f...
  • Senior Medical Advisor
    Biotech / Pharmaceuticals
  • Leading Pharmaceutical Company
  • Southampton, Hampshire
  • 03/05/12
  • To be an expert on the ABPI code of practice and to ensure and monitor company compliance with the codes and other company policies, Be responsible f...
  • A forensic scientist with DNA specialisation and court experience as an expert witness. Responsible for high throughput reporting of NDNAD matches and...
  • 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 ...
  • As the Global Auditor Manager you will be joining their global operational excellence team and you will focus on Quality engineering, Global audit man...
  • Manage assigned geographic territory with regard to sales activities, including: Generate product interest and lead generation by performing cold call...
  • The FSE will act as an essential interface between the field organization and internal support structure by providing timely onsite technical assistan...
  • 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...
  • 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. ...
  • This ADQAA will have responsibility for management of the global auditing team, which currently sits at 10 staff across UK, US, Germany, Spain, Italy ...
  • The GPM will be responsible for managing International studies in Phases I-IV. This is a client focused role which is pivotal in the success of our pr...
  • CRA Line Manager
    Biotech / Pharmaceuticals
  • Chiltern International Holdings
  • United Kingdom
  • 01/05/12
  • The successful candidate will be expected to know Allergan systems and SOPs to a good level, and really focus on CRA performance / generate metrics /...
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