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Job description
Bristol Myers Squibb seeks an Associate Director in Regulatory Affairs to spearhead global strategy and filings for Heme/Onc products. You will drive IND/NDA submissions, coordinate with clinical and commercial teams, and ensure compliance with HA timelines.
The role requires leadership in cross-functional teams, extensive FDA experience, and a strong regulatory science background to enable timely development and life-cycle planning.
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Worksite address
princeton, NJ, 08543, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.