All jobs
Principal Medical Writer
ICON plc
Frankfurt +4 · Remote possibleSenior (5–10 years)Full-timePosted 21 Aug 2026
About the job
What you'll do
Lead the development of high-quality regulatory and clinical documents to support submissions to global regulatory authorities. Manage medical writing projects, including timeline development and cross-functional coordination to ensure compliance with industry standards.
What they're looking for
Requires a Bachelor's degree in life sciences and at least 6 years of medical writing experience within the biopharmaceutical or CRO industry. Must be proficient in regulatory writing for Clinical Study Reports and Protocols, with oncology experience preferred.
Full description