About this opportunity
Bristol-Myers Squibb Co lists this Regulatory Project Lead – Biotech Radiopharma opportunity in indianapolis, Indiana. Review the employer’s description below for duties, qualifications and application requirements.
Job description
RayzeBio, 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.
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Worksite address
indianapolis, IN, 46262, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.