Regulatory Project Lead – Biotech Radiopharma
Regulatory Project Lead – Biotech Radiopharma
bristolmyers squibbIndianapolis, IN
yesterday
Research and Development in Biotechnology (except Nanobiotechnology)Biological Product (except Diagnostic) ManufacturingElectromedical and Electrotherapeutic Apparatus Manufacturing
Apply for this role →Rayze Bio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks a Manager of Regulatory Project Management to lead global regulatory submissions across oncology programs. You will manage cross-functional timelines, deliverables, and communication to ensure timely, high-quality submissions.
Reports to Head of Regulatory Project Management. The role requires 5+ years in regulatory affairs or healthcare and a strong background in major submissions (NDA/IND) with radiopharmaceutical exposure.
Also on the board Same function, level within a rung
Level
Manager
Location
Indianapolis, IN
Occupation
Regulatory Affairs Managers
Industry
Research and Development in Biotechnology (except Nanobiotechnology)
Posted
yesterday