Medical Writer

Clinical Medical Writer - (UK/Europe-Based, Remote) - 0.6 FTE Contract We are currently hiring a Medical Writer to join a regulatory writing team, with a particular focus on WHO submissions and ATC classification work. This is a remote, home-based role open to candidates anywhere in the UK or Europe, offered on a 0.6 FTE contract basis. Role Overview You will be responsible for preparing, reviewing, and quality-checking regulatory and scientific documentation supporting WHO submission activities. You'll work closely with Regulatory Affairs, Clinical, and Pharmacovigilance teams. Experience Required 2-3 years' medical writing experience within pharma, biotech, or a regulatory consultancy environment Proven track record producing high-quality clinical and regulatory documents to tight timelines Experience working with global regulatory frameworks, ideally including WHO submission pathways Familiarity with ATC classification and verification

Comfortable interpreting and synthesising complex clinical and scientific data for varied audiences Strong attention to detail, with experience in document QC, version control, and referencing Confident liaising with cross-functional stakeholders including Regulatory Affairs, Clinical, and Pharmacovigilance Right to work in the UK or EU Able to work independently and manage priorities in a remote, part-time contract role