Lead Principal Medical Writer — Regulatory & Clinical Docs

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.

• 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