Medical Writer III (Pharmacovigilance)

We are looking for an experienced pharmacovigilance medical writer to join our growing medical writing team.
What We're Looking For: 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. You will play a key role in delivering high-quality regulatory documents, strengthening client relationships, and supporting the growth of the wider team. The Medical Writer will be responsible for medical writing including:
Key Responsibilities:
Author, review, and quality check a range of regulatory and pharmacovigilance documents, including:
PSURs/PBRERs
PADERs
ACOs
DSURs
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 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 to support their professional growth and development.
Contribute to process improvements and the continuous enhancement of medical writing quality standards.
MD, pharmacy or Life Science degree (Masters or PhD is desirable)
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, an additional language is a benefit

Employment type
Full-time

Work arrangement
Yes