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
Regulatory Medical Writer II - Lead Complex Clinical Docs in Maidenhead employer: Fortrea
Fortrea is an exceptional employer that offers a rewarding and meaningful work environment, particularly for Senior Technical Designers. With a strong support network, flexible working solutions, and a commitment to employee growth, you will thrive in a collaborative workspace that values diversity and inclusion. Enjoy competitive compensation packages and the opportunity to make a significant global impact while maintaining a genuine work-life balance.
