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Manager, Global Scientific and Regulatory Documentation at Bristol Myers Squibb

Setup
Hybrid
Type
Full-time
Level
not_specified

Description

This role involves leading and providing strategic direction for end-to-end documentation specialists in regulatory filings, HA responses, and complex clinical protocols. Responsibilities include managing eDMS processes, submission-readiness formatting, PDF processing, and publishing of regulatory documents. The specialist will also lead training, troubleshoot issues, collaborate with cross-functional business partners, define submission-ready requirements, and participate in continuous improvement initiatives.

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