Regulatory Medical Writer II — Lead Complex Clinical Docs

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

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