Principal Medical Writer

The Principal Medical Writer will support 4D-150, a gene therapy in late-stage development for retinal vascular diseases, including nAMD and DME, and associated BLA-enabling activities as well as clinical stage work within the lung program. This role is responsible for the planning, development, and delivery of high-quality clinical and regulatory documents across late-stage development, working closely with Clinical Science, Clinical Operations, Data Science, Regulatory Affairs, Quality, and external partners.

Requirements

• 5+ years of medical or clinical writing experience in biotech, pharmaceutical, or CRO settings
• Direct experience supporting Phase 3 clinical trials required; direct experience supporting early clinical trials (Phase 1/2) preferred
• Prior experience authoring or contributing to BLA-enabling documents strongly preferred
• Advanced degree in life sciences (MS, PhD, PharmD, MD) preferred; Bachelor's degree required

Benefits

• Generous Paid Time Off
• 401k Matching
• Retirement Plan