Medical Writer

Join our Medical Writing team and play a key role in delivering high-quality scientific and regulatory documents that support clinical development programmes worldwide. As a Medical Writer (Consultant), you will lead and contribute to a variety of medical writing projects, collaborating with cross-functional teams and clients to ensure the delivery of accurate, compliant, and impactful documentation. You will also act as a subject matter expert, providing guidance to colleagues and supporting continuous improvement across the function. What You'll Do Medical Writing & Document Development Author, review, and quality-check a range of regulatory and scientific documents, including clinical study reports and other medical writing deliverables. Ensure all documents accurately reflect source data, meet regulatory requirements, and comply with company and client standards. Manage document review cycles, resolve reviewer comments, and coordinate feedback from multiple stakeholders. Provide editorial support, proofreading, and quality control reviews where required. Support document publishing activities and compilation of submission-ready deliverables. Project Leadership & Delivery Manage multiple writing projects simultaneously, ensuring delivery within agreed timelines and budgets. Track project milestones, risks, and progress using project management tools. Collaborate closely with project teams, reviewers, and subject matter experts to ensure efficient project execution.