Medical Writer III, Pharmacovigilance

• Author, review, and quality check regulatory and pharmacovigilance documents, including PSURs/PBRERs, PADERs, ACOs, DSURs, and 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
• Act as a trusted point of contact for clients and support project delivery
• Foster strong working relationships with clients
• Provide guidance, mentoring, and knowledge sharing to junior medical writers
• Support professional growth and development of Associate Medical Writers
• Contribute to process improvements and enhancement of medical writing quality standards

• 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
• Strong team-player skills
• Fluency in English
• Additional language is a benefit
• Experience with regulatory and pharmacovigilance writing
• Client-focused mindset and attention to detail

• Remote work option
• Professional growth and development opportunities
• Mentoring and knowledge-sharing opportunities
• Collaborative and supportive work environment
• Flexible work culture
• Belonging and inclusive workplace culture
• Opportunity to contribute to patient safety and global pharmaceutical work