The Medical Writer position with PrimeVigilance offers an opportunity to further develop your career in Pharmacovigilance Medical Writing. PrimeVigilance’s Medical Writing team is based in North America, Europe and Asia.

Key Accountabilities

  • Author Medical Writing tasks including aggregate reports, RMPs and other documents needed throughout the product’s life cycle
  • Responsible for the quality and content of the document, and quality control review of documents prepared by Medical Writing peers
  • Continuous self-education in all aspects associated with Medical Writing activities
  • Active participation in trainings, maintenance, and development of quality system documents
  • Support in all PV operations associated with Medical Writing


  • PhD or MSc in Life Sciences or Healthcare (pharmacy, biology, chemistry, veterinary medicine)
  • Previous experience of drug safety medical writing, including PBRERs, DSURs, RMPs
  • Time management, organisation and multitasking skills with good attention to detail
  • Strong communication and presentation skills
  • Advanced knowledge of MS Office
  • Fluency in English