Senior Medical Writer – Regulatory Dossier Lead

GSK is looking for a Principal Medical Writer based in Stevenage. The candidate will manage complex regulatory writing projects and deliver high-quality clinical documents for global submissions. This role involves independent authorship and collaboration within cross-functional teams to ensure compliance with regulatory standards.

The ideal candidate should have a PhD or equivalent experience, advanced regulatory writing skills, and a strong grasp of clinical trial design. GSK offers a hybrid working model, competitive salary, annual bonus, and comprehensive healthcare benefits.

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