Senior/Principal Medical Writer: Early-Phase Regulatory Expert

ProPharma is seeking a Senior/Principal Medical Writer based in the UK or Ireland. The role focuses on authoring regulatory and clinical documents across phases, with leadership in delivery quality and timelines.

You will collaborate with cross-functional teams and mentor junior writers to maintain high standards. Ideal candidates have 7+ years of clinical/regulatory writing experience, strong knowledge of FDA/regulatory guidelines, and excellent communication and project-management skills.