Director, Medical Writing

Director, Medical and Regulatory Writing

*Hybrid Role - Menlo Park, CA*'

Meet has partnered with an exceptional Bay Area pharma focused in treatments for metabolic, psychiatric, and oncologic disorders. Our client has an approved product and a dynamic late-stage pipeline. They are looking for a Director of Medical/Regulatory Writing to join their team - this role will be reporting directly into the VP of Regulatory Affairs.

Key Responsibilities

You will lead the authoring of clinical/nonclinical documents (CSR, IB, DSUR)

You will manage the development of key regulatory submissions (IND/CTA/NDA/MAA)

You will work to author, edit, review, and process major submissions

Key Qualifications

8+ years of relevant industry experience required

Advanced degree (PhD, PharmD, MS) preferred

Experience leading the authoring of a variety of technical documents

Please reach out directly to Ryan Moran to learn more: