The PrimeVigilance Medical Writer position offers an opportunity to further develop your career in the field of Pharmacovigilance Medical Writing.

Key Accountabilities

  • Independent authoring, editing, and reviewing of various regulatory/clinical documents (e.g. aggregate reports, risk management plans, and other documents needed throughout the product’s life cycle) with the responsibility for the quality and content of the document and compliance with internal and external standards
  • Active participation in training and development, implementation and maintenance of quality system documents for medical writing, including internal templates and formats required for standardized documentation
  • Support in all pharmacovigilance operations associated with medical writing
  • Continuous self-education in all aspects associated with medical writing


  • Previous experience of pharmacovigilance medical writing, including PBRERs, DSURs, RMPs 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

  • A dynamic team of colleagues in a fast-growing company – possibility for quick career growth
  • Multicultural environment, English as a company language
  • Strong emphasis on personal and professional growth
  • Friendly working environment

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