Regulatory Project Lead – Biotech Radiopharma

L7

bristolmyers squibbIndianapolis, INyesterday
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.
Apply now
Apply now

Level

ManagerL7

Location

Indianapolis, IN

Occupation

Regulatory Affairs Managers

Industry

Research and Development in Biotechnology (except Nanobiotechnology)

Posted

yesterday

To get sharper similar jobs, create your profile using the link below.

Create profile