Senior Medical Writer Pharmacovigilance - London, United Kingdom - X4 Group

X4 Group
X4 Group
Verified Company
London, United Kingdom

3 weeks ago

Tom O´Connor

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Tom O´Connor

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Description
Looking for your next contract role?

A leading Pharmaceutical Consultancy are looking for a Regulatory Medical Writer with Pharmacovigilance experience to join them in January.


You will be expected to author Pharmacovigilance safety reports: PSUR, PBRER, PADER, RMP, ACO, etc., Author and prepare clinical documentations, and act as a project lead.


Outline:

  • Fully remote.
  • 6month contract.
  • Flexible pay rate (DOE).


You are required to have at least 2 years of experience within the pharmaceutical industry working in a pharmacovigilance department or have experience writing aggregate reports.

Familiarity with drug safety, drug development and pharmacology is essential.
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