Lead Principal Medical Writer — Regulatory & Clinical Docs
Full-time
Barrington James
Urgent Permanent Principal Medical Writer | France, UK, Spain, Germany
*ONLY APPLICANTS FROM THESE COUNTRIES WILL BE CONSIDERED*
We are supporting a global clinical research organisation seeking a Senior / Principal Medical Writer to join a growing international medical writing team. You will lead the development of key clinical and regulatory documents including protocols, CSRs, IBs, and submission materials, ensuring scientific accuracy and compliance with ICH-GCP, FDA, and EMA guidelines.
Working closely with global teams across clinical operations, biostatistics, regulatory affairs, and medical affairs, you will translate complex clinical data into high-quality regulatory and publication‑ready outputs. The role also includes mentoring junior writers.
Requirements
- 4–7+ years’ medical writing experience (CRO, pharma, biotech)
- Strong clinical/regulatory documentation expertise
- Ability to interpret complex clinical and statistical data
- Experience in fast‑paced, multi‑project environments
Location: France, UK, Spain, Germany
#J-18808-LjbffrVacancy posted 2 days ago
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