Medical Writer III, Pharmacovigilance
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Job Description
Medical Writer III creating regulatory pharmacovigilance documents for PrimeVigilance, a global patient-safety specialist. Analysing safety data, supporting clients, and mentoring junior medical writers.
Responsibilities:
- Author, review, and quality check regulatory and pharmacovigilance documents, including PSURs/PBRERs, PADERs, ACOs, DSURs, and Risk Management Plans (RMPs)
- Ensure documents are scientifically accurate, regulatory compliant, and delivered within agreed timelines
- Collaborate with cross-functional teams to analyse, interpret, and present safety data
- Act as a trusted client point of contact, supporting project delivery and fostering working relationships
- Provide guidance, mentoring, and knowledge sharing to junior medical writers
- Contribute to process improvements and enhancement of medical writing quality standards
Requirements:
- MD, pharmacy, or Life Science degree
- Minimum 2 years' experience in Medical Writing and associated fields (case processing, signal detection, or risk management)
- Experience ideally within a CRO environment
- Ability to manage multiple and varied tasks and prioritize workload with attention to detail
- Ability to effectively train and mentor Associate Medical Writers
- Strong team player
- Fluency in English
- Additional language is a benefit
- Master's or PhD is desirable
Benefits:
- Remote work option
- Flexible work environment
- Growth and professional development opportunities
- Mentoring and knowledge-sharing opportunities
- Collaborative team environment
- Belonging-focused workplace culture
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