Senior/Principal Medical Writer — Author Clinical Documents for Global Drug Development (Remote)

The Role

Precision Medicine Group is hiring a Senior Medical Writer / Principal Medical Writer to lead the development of high-quality, on-time clinical study documents — from protocols and investigator brochures to DSURs, CSRs, and patient narratives. Fully remote.

What You'll Do

• Plan, write, edit, format, and QC clinical documents across all phases of development
• Ensure every document complies with regulatory guidelines (ICH, FDA, GCP) and eCTD requirements
• Collaborate with cross-functional teams to deliver accurate, submission-ready content
• Bring impeccable attention to detail to complex, high-stakes documentation

Who You Are

You have deep experience writing clinical documents in pharma, biotech, or a CRO — and a clear understanding of regulatory content requirements across development phases. You're a strong communicator who thrives on precision and can manage multiple projects without dropping the ball.

Why Precision

A role where craft matters — your words go into regulatory submissions that shape global drug development. Remote flexibility, meaningful work, and a team that values scientific rigor.

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