https://jobs.co.uk/job/medical-writer-regulatory-hays-life-sciences--e804d077-b703-477b-b2a7-859c1f68771d RSS feed for Medical Writer (Regulatory) at Hays Life Sciences. en-gb Thu, 02 Jul 2026 03:37:10 GMT https://jobs.co.uk/job/medical-writer-regulatory-hays-life-sciences--e804d077-b703-477b-b2a7-859c1f68771d https://jobs.co.uk/job/medical-writer-regulatory-hays-life-sciences--e804d077-b703-477b-b2a7-859c1f68771d Tue, 30 Jun 2026 23:00:00 GMT Location: City of London | Salary: £40.00 - £55.00/hour £40 - £55 p/h OUTSIDE IR35 | Type: Contract | Your new company We are seeking an experienced Medical Writer with strong regulatory expertise to support a rapidly growing Regulatory Affairs consultancy. They count some of the biggest multinational pharmaceutical companies as clients and continue to provide regulatory solutions that drive success.This is a fully remote, UK-based contract opportunity (outside IR35), ideal for a consultant with a proven track record in regulatory submission documents. Your new role Author, review, and edit regulatory documents in line with global submission requirements. Update existing documents: Clinical Overview (Module 2.5) and Clinical Summary (Module 2.7) documents. Collaborate cross-functionally with clinical, regulatory, and biostatistics teams. Ensure consistency, scientific accuracy, and compliance with ICH guidelines. Manage document timelines and incorporate feedback from multiple stakeholders. Support preparation for regulatory submissions (e.g. CTD/eCTD). What you''ll need to succeed Several years'' experience in medical writing within the pharmaceutical or biotech industry. Demonstrable expertise in Modules 2.5 and 2.7 (Clinical Overview and Clinical Summary). Stron... Contract