At Fortrea, we help bring life‑changing treatments to patients faster. We are seeking an experienced Senior Regulatory Medical Writer to lead the development of high‑complexity clinical regulatory documents in partnership with a leading global pharmaceutical company.

What You Will Do

As a sponsor‑embedded Regulatory Medical Writer, you will lead the full development lifecycle of Phase II–IV clinical regulatory documents, with primary responsibility for:

• Clinical Protocols
• Investigator’s Brochure (IBs)
• Submissions

You will own document development from planning through final delivery, including:

• Leading kick‑off, communication, and comment‑resolution meetings
• Coordinating cross‑functional contributors and reviewers
• Maintaining alignment with sponsor goals, timelines, and milestones
• Interpreting clinical data and translating results into clear, compliant regulator...