Principal Medical Writer – Regulatory Submissions (Hybrid)

GSK in Stevenage, United Kingdom is seeking a Principal Medical Writer to author high-quality regulatory documents such as protocols, CSRs, Investigator’s Brochures, and CTD submission documents. Hybrid work model combining remote and on-site collaboration.

You will lead planning and delivery of clinical dossier documents for global submissions, ensuring quality, consistency, and timeliness while coordinating cross-functional teams.

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