https://jobs.co.uk/job/senior-medical-writer-pharmacovigilance-hays-life-sciences--96139dfe-1920-4e1f-a509-e4d6edd7860c RSS feed for Senior Medical Writer, Pharmacovigilance at Hays Life Sciences. en-gb Fri, 10 Jul 2026 16:10:09 GMT https://jobs.co.uk/job/senior-medical-writer-pharmacovigilance-hays-life-sciences--96139dfe-1920-4e1f-a509-e4d6edd7860c https://jobs.co.uk/job/senior-medical-writer-pharmacovigilance-hays-life-sciences--96139dfe-1920-4e1f-a509-e4d6edd7860c Fri, 10 Jul 2026 11:52:38 GMT Location: Hertfordshire | Salary: 10000-500000 Annual | Type: Contract | Your new company Are you an experienced Senior Medical Writer looking for your next long-term contract opportunity?I am currently partnering with a leading global pharmaceutical organisation seeking a Senior Medical Writer to join their clinical and regulatory writing team on an initial 12-month contract.This role sits within a high-performing global team and will suit a writer who is confident leading the development of complex regulatory and safety documentation whilst collaborating with cross-functional stakeholders across Clinical Development, Pharmacovigilance, Regulatory Affairs, Biostatistics and Medical Affairs.Your new role Lead the preparation, review and delivery of high-quality clinical and regulatory documents.Author and coordinate clinical study protocols and protocol amendments.Develop Pharmacovigilance and aggregate safety reports including:DSURs (Development Safety Update Reports)PBRERs (Periodic Benefit-Risk Evaluation Reports)Prepare clinical study reports, investigator brochures and other regulatory submissions as required.Support documentation associated with medical devices and combination products, ensuring compliance with relevant regulatory requirements.Col... Contract