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Regulatory Medical Writer II - Lead Complex Clinical Docs
Posted 2 days ago by Fortrea
Permanent
Full Time
Other
Berkshire, Maidenhead, United Kingdom, SL6 0
Job Description
Fortrea is seeking a Regulatory Medical Writer II to own high-complexity Phase II IV clinical regulatory documents and manage lifecycle from planning to final delivery, closely coordinating with cross functional teams. You will author protocols, ICFs, investigator brochures, and briefing packages, while leading planning, reviews, and approvals across geographically distributed teams.
The role requires at least 3 years in regulatory medical writing, strong science communication, and knowledge of
Fortrea
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