‼️ 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
Email me your CV [click apply] 📥