• Author medical writing tasks, including aggregate reports, Risk Management Plans (RMPs), and other documents throughout the product’s life cycle.
• Responsible for the quality and content of documents, as well as quality control review of documents prepared by medical writing peers.
• Engage in continuous self-education regarding all aspects of medical writing activities.
• Actively participate in training sessions, maintenance, and development of quality system documents.
• Support pharmacovigilance operations associated with medical writing.
• PhD or MSc in Life Sciences or Healthcare (e.g., pharmacy, biology, chemistry, veterinary medicine).
• Previous experience in drug safety medical writing, including PBRERs, DSURs, and RMPs.
• Strong time management, organization, and multitasking skills with excellent attention to detail.
• Strong communication and presentation skills.
• Advanced knowledge of MS Office.
• Fluency in English (both verbal and written).
• PrimeVigilance offers an opportunity for medical writers to further develop their careers in pharmacovigilance medical writing.
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