Remote UK Lead Medical Writer – Regulatory Excellence

Mms is seeking a full-time Medical Writer to work remotely within the UK. The candidate will critically evaluate literature, write and edit regulatory documents (protocols, brochures, CSRs, ICH modules), and manage timelines for multiple projects.

Ideal candidates have 3+ years in pharma, 3–5 years of regulatory/clinical writing, and strong leadership and communication skills. Experience with orphan drug designations is a plus.

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