Medical Writer III (Pharmacovigilance)

We are looking for an experienced pharmacovigilance medical writer to join our growing medical writing team. A highly motivated and detail-oriented medical writer who combines strong regulatory writing expertise with a client-focused mindset and a passion for developing others.

Responsibilities

Author, review, and quality check a range of regulatory and pharmacovigilance documents (PSURs/PBRERs, PADERs, ACOs, DSURs, Risk Management Plans); Ensure documents are scientifically accurate, regulatory compliant, and delivered within agreed timelines; Collaborate with cross-functional teams to analyse, interpret, and present safety data effectively; Act as a trusted point of contact for clients, supporting project delivery and fostering strong working relationships; Provide guidance, mentoring, and knowledge sharing to junior medical writers; Contribute to process improvements and the continuous 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) 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; Must be a strong team player; Fluency in English

Nice to have

Masters or PhD is desirable; Additional language is a benefit