Public summary
We are seeking an experienced Senior Medical Writer to join a leading mid-size CRO in Europe. This full-time role can be based in several European countries including Germany. The role involves writing and editing complex medical documents such as clinical study reports, protocols, and regulatory submissions, while coordinating cross-functional teams to ensure scientific accuracy and compliance. Candidates should have a degree in Life Sciences, at least three years of medical writing experience, strong project management skills, and fluency in English.
Location and work setup
- Location
- Mannheim
- Remote status
- Hybrid
- German requirement signal
- No German Required Detected
- Detected job language
- English
Responsibilities
Write and edit complex medical writing deliverables according to SOPs and regulatory guidelines; coordinate with multiple departments to ensure timely collection and review of scientific content; ensure accuracy, consistency, and compliance of all documents; conduct quality control reviewing data accuracy and formatting; mentor and lead junior writers; liaise with sponsors to align on deliverables.
Qualifications
Degree in Life Sciences; minimum three years of medical writing experience including protocols, clinical study reports, and CTD submissions; fluent in English; project management and coordination skills; experience in a CRO setting is a plus.