Senior Medical Writer – Remote UK, Regulatory & Protocol

MMS is seeking a senior Medical Writer to join a remote UK-based team. The role focuses on evaluating literature, writing and editing regulatory documents, and leading writing projects to support clinical development and regulatory submissions.

Ideal candidates have 3+ years in pharma regulatory writing, strong MS Word skills, and a scientific/medical background (Bachelor/Master/PhD). Excellent writing, organization, and leadership abilities are essential.

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