Bristol Myers Squibb in Princeton, NJ, seeks an Associate Director, Global Scientific and Regulatory Documentation, Content Strategy, to coordinate and author complex regulatory documents for global submissions. The role spans immunology and cardiovascular assets, driving document strategy, timelines, and cross-functional collaboration to ensure compliant, high-quality submissions.
The ideal candidate will bring expert regulatory writing skills, experience with registrational documents, and a
#J-18808-LjbffrGlobal Regulatory Documentation Lead in princeton at Unknown Company
This position is listed as full time and onsite.