Document Writer – Edinburgh

A document writer in Edinburgh supports the creation of clinical research and regulatory documents, including protocols, reports, and consent forms. The role requires ensuring compliance with global regulatory standards such as ICH GCP and collaborating with stakeholders to maintain high-quality documentation. Responsibilities include editing, reviewing, and managing technical documents, liaising with clients and third-party consultants, and supporting process improvements. Candidates should possess excellent writing skills, attention to detail, and familiarity with clinical research practices. The position involves working with Microsoft Office tools, maintaining regulatory compliance, and managing multiple projects efficiently. It offers opportunities to develop expertise in regulatory scientific documentation within the life sciences industry.