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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Senior Medical Writer - Early-Phase Clinical & Regulatory employer: propharmagroup
ProPharma is an exceptional employer that fosters a collaborative and innovative work culture, particularly for those in the Global Life Sciences sector. With a strong focus on employee growth and development, team members benefit from flexible hybrid working arrangements that promote work-life balance while engaging in meaningful projects that impact the industry. Join us to be part of a dynamic team dedicated to excellence in talent acquisition and make a real difference in the lives of professionals across Quality & Compliance, Regulatory Sciences, and more.
