Drug Safety Scientists Jobs

Drug Safety ScientistsWe handle many vacancies for experienced Drug Safety Scientists. Below you'll find an examples of typical Drug Safety Jobs. Login to find our current vacancies.
Our client, a leading global contract research organisation with offices throughout Europe, the USA, Asia Pacific, South America and South Africa, has an opening for an experienced pharmacovigilance professional to join their medical safety team as a Drug Safety Monitor based in the South of England. In this r�le you will be responsible for tracking and processing adverse events and other drug safety information from clinical trial and post marketing surveillance projects. You will work closely with the clinical development, data management and regulatory departments to ensure that all adverse events are communicated to the applicable regulatory authorites within the UK and overseas. The successful candidate will have a life science degree or relevant qualification and at least one years experience in a drug safety r�le. Experience of reporting SAEs within a European/global environment would be a distinct advantage. You must be a good communicator and confident dealing with industry professionals of all levels. There is an attractive remuneration package on offerto the right candidate including pension, healthcare, life assurance and holday pay. This is an excellent opportunity to gain pharmacovigilance experience within the European environment and is not to be missed! Call us today to discuss this opportunity in the strictest of confidence.

A leading pharmaceutical company has an urgent requirement for an experienced Drug Safety Officer to complement their existing safety reporting group based in the South East on a short term contract. You will be responsible for the identification, reporting and follow up of serious adverse events on a worldwide level for a number of products across several therapeutic areas. There is a competitive hourly rate available to the successful candidate plus holiday pay and other negotiable benefits. This is an excellent opportunity to consolidate further your exisiting pharmacovigilance experience within a blue chip pharma environment!

The successful candidate will have a minimum of 1-2 years' experience in a similar r�le within a pharmaceutical company co-ordinating SAE's from both clinical trials and marketed products.
Gain more experience within pharmacovigilance!This is a great opportunity to join a well respected international contract research organisation entering an exciting period of growth, as a Drug Safety Associate. In this r�le you will project manage the reporting of spontaneous and serious adverse events to European regulatory authorites for investigational and marketed products in phases II-IV of development. There will be an element of database management with this r�le to ensure that all serious adverse events are resolved and updated in accordance with the appropriate guidelines. There will be the opportunity to gain experience within a wide range of therapeutic areas while building upon existing drug safety experience. The successful candidate will have a minimum of one years experience in drug safety combined with previous experience within the pharmaceutical industry in a similar r�le. A BSc in life science or related area is required for this position. Please call us for a confidential discussion about this position and take the first step towards joining an organisation committed to the personal development and training of its employees!

Latest clinical research jobs

Login for all our vacancies

Call us on +44(0)1279 657716