Associate Director, Regulatory Medical Writing
Regeneron Pharmaceuticals(8 days ago)
About this role
An Associate Director of Medical Writing at Regeneron leads medical documentation efforts for specific compounds, managing teams and overseeing regulatory submissions. The role involves strategic planning, process improvement, and ensuring adherence to guidelines within a collaborative environment. It requires extensive clinical writing expertise and leadership skills to impact patient lives positively.
Required Skills
- Medical Writing
- Regulatory Submissions
- Clinical Documentation
- Leadership
- Project Management
- ICH GCP
- Document Management
- Strategic Planning
- Adobe Acrobat
- Microsoft Word
Qualifications
- Bachelor’s Degree
- 8+ Years Relevant Experience
- Advanced Degree Preferred
- Expert Knowledge of Clinical Research & Regulations
About Regeneron Pharmaceuticals
regeneron.comDiscover how Regeneron (NASDAQ: REGN) harmonizes biology and technology to create life-changing medicines. Join our team and explore clinical trials.
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