Upvote
Downvote
Associate Director, CMC Regulatory Affairs
Share Job
- Suggest Revision
- Associate Director, CMC Regulatory Affairs is a hands-on and independent role requiring a strong individual who will provide strategic and operational support to multiple programs, with an emphasis on CMC (Chemistry, Manufacturing, and Controls).
- This role will assist with global clinical trial applications, global marketing applications (including US, Europe, Canada, Rest of World, etc.)
- Leads and support the development and implementation of CMC regulatory strategy to support global development programs and market applications.
- Responsible for ensuring the appropriate execution of CMC regulatory strategy.
- Ensures the effectiveness of the CMC Regulatory team in developing submissions and in working across functions (such as Drug Product Development, Drug Substance Development, Analytical/QC, and Quality teams).
Active Job
Updated YesterdaySimilar Job
Relevance
Active