Associate Director, Medical Writing

The Associate Director, Medical Writing will develop and finalize clinical and regulatory documents supporting Summit Therapeutics’ oncology development programs. Responsibilities include authoring protocols, clinical study reports, Investigator’s Brochures, briefing materials, and clinical summary documents while ensuring accuracy and regulatory compliance. The role coordinates cross-functional contributions, review schedules, comment resolution, and on-time delivery across global teams. This position also helps improve medical writing processes, templates, and standards in a fast-paced environment.