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 :
ryan.moran@peoplewithchemistry.com
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