Senior Medical Writer – Early-Phase Clinical & Regulatory

ProPharma is seeking a Senior or Principal Medical Writer based in the UK or Ireland to support a top pharmaceutical client, delivering high‑quality medical writing across clinical and regulatory documents.

The role requires a minimum of 5 years’ experience in writing clinical/regulatory deliverables, fluency with FDA/ICH guidelines, and the ability to mentor junior writers while coordinating with cross‑functional teams in a hybrid work setting.

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