Bristol Myers Squibb in Princeton, NJ seeks an Associate Director, Global Regulatory Sciences - CMC to lead content development and review of the Quality Module for global regulatory submissions, including clinical trial applications, new marketing applications, and post-approval packages.
You will partner with GPS and CTDO, guide change management, interface with Health Authorities, and supervise cross-functional teams to ensure timely, compliant CMC submissions across markets.
#J-18808-LjbffrGlobal Regulatory CMC Associate Director: Strategy Lead in princeton at Unknown Company
This position is listed as full time and onsite.