TransPerfect is seeking an experienced Medical Writer in the UK to lead the development of regulatory and clinical study documents. The role involves managing timelines, coordinating across client teams and internal resources, and ensuring compliance with client processes and templates.
The ideal candidate has 5+ years in medical writing for CRO/biotech/pharma, a relevant bachelor’s degree, and experience with study reports, protocols, and regulatory documents, including ICH standards.
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Senior Medical Writer - Clinical Documentation Lead employer: TransPerfect
TransPerfect is an exceptional employer that fosters a vibrant and innovative work culture, perfect for ambitious individuals looking to thrive in the fast-paced language services industry. With a strong commitment to employee growth, we offer structured leadership development pathways and uncapped commission opportunities, ensuring that your hard work translates into meaningful career advancement. Located in London, our diverse team celebrates unique perspectives, making it an ideal environment for those eager to make a significant impact while building lasting client relationships.
