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Drug Safety Officer - 6 month contract

An excellent opportunity has become available for a Pharmacovigilance (PV) Officer / Associate to join an exciting team based in Oxford.

Within this role you will be responsible for facilitating and supporting the global review of departmental documents, ensuring the records are handled & maintained in compliance with the Company's SOPs and records management policies, as well as legal and regulatory requirements.

Responsibilities:

, Review and organize the PV departmental electronic and hard copy files and update various document storage repositories and databases as needed
, Complete document clean-up activities as required following review of the PV departmental files
, Work closely with departmental SMEs to identify and classify a variety of document types
, Track document assessment and disposition accurately and on a continuous basis
, Work with departmental SMEs to perform and support the clean-up of case data in the Safety Database.
, Requires the ability to work both independently and in collaboration with the global teams
, Other duties as assigned

Experience Required:

, 2 + years' experience working in a pharmacovigilance role, with exposure to both clinical and post-marketing safety data
, Knowledge of PV quality assurance activities preferred
, Ability to multi-task and shift priorities
, Exceptional organizational skills
, Ability to communicate effectively, both verbally and in writing
, Works efficiently with little supervision
, Familiarity with the Argus pharmacovigilance database strongly preferred.

For further information about this role, please contact Tim Barratt on +44(0)1727 817 626 or email a copy of your CV to tbarratt@keypeople.co.uk


  • Start: asap
  • Duration: 6 months
  • Location: Oxfordshire, England
  • Type: Contract
  • Industry: Pharmaceutical
  • Recruiter: Key People
  • Tel: +44 (0)1727 817 626
  • Fax: 01727 844 838
  • Email: to view click here
  • Posted: 2020-02-19 22:09:06 -

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