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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.
Job Responsibility:
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
Requirements:
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
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