We are seeking an experienced medical writer with deep expertise in clinical and regulatory documents and demonstrated experience using AI-enabled tools to support the development, review, and quality control of clinical documentation. This individual will contribute to the preparation of high-quality documents such as clinical study protocols, clinical study reports, investigator’s brochures, protocol amendments, regulatory briefing materials, and related clinical documents, while also helping to define efficient, compliant, human-in-the-loop workflows for AI-assisted document generation. The ideal candidate combines strong scientific and regulatory writing judgment with practical experience using generative AI, automation, structured content reuse, and/or document intelligence tools to improve speed, consistency, and quality in medical writing deliverables.
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Job Type
Full-time
Career Level
Director
Education Level
No Education Listed