The PrimeVigilance medical writer position offers a unique opportunity to further develop your career in the field of drug safety.

We are looking for an experienced pharmacovigilance medical writer to join our team. The Medical Writer will be responsible for medical writing including:

  • PADERs
  • ACOs
  • DSURs
  • RMPs
  • CSEs
  • Signal detection reports
  • PSMF
  • QC and review of all written output from the operations team as required
  • Supporting the project managers to determine scheduling of the aggregate reports for which they are responsible
  • In conjunction with the Quality, Compliance and Training Manager identify areas for improvement and address via training, clarifying changes to SOPs/OGs/templates
  • Complete quality documentation of aggregate reports
  • Attending kick off meetings with new clients as required
  • Attending audits and inspections as required
  • Providing aggregate report training


  • 3 years’ experience of pharmacovigilance medical writing, including 2 years PSUR writing
  • Life Science degree, or have equivalent nursing or medical qualifications
  • Ability to manage multiple and varied tasks and prioritize workload with attention to detail
  • Ability to effectively train and mentor Associate Medical Writers
  • Advanced knowledge of English

Our Offer

  • Competitive salary
  • Dynamic team of colleagues in a fast-growing company – possibility for your quick career growth
  • Multicultural environment, English as a company language
  • Strong emphasis on personal and professional growth
  • Extensive and specialized trainings in pharmacovigilance – internal trainings provided by skilled professionals, but also prestigious trainings/seminars taking place abroad
  • Friendly working environment with several social events per year

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