Associate Director, Regulatory Affairs Medical Writing
beelinemedicines · United States
- Posted
- 59 days ago
- Last confirmed live
- Today
What this role involves
The Associate Director, Regulatory Affairs Medical Writing is responsible for authoring and coordinating high-quality regulatory and scientific documents for a biotechnology company's pipeline. The role involves hands-on writing, operational leadership of medical writing activities, and collaboration with cross-functional teams to support IND, BLA/NDA submissions. The position is remote with periodic travel to company offices.
Skills this posting asks for
- medical writing
- regulatory submissions
- clinical study reports
- protocol writing
- investigator brochures
- regulatory documents
Requirements
- Level: director
- Remote policy: hybrid
From the employer’s posting
About Beeline Medicines: Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people livi…
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