Director, Early Precision Medicine Regulatory Affairs
Bristol Myers SquibbNew Jersey, United States • New Jersey, United States • New Jersey, United States
Posted October 27, 2025
217960 - 264113 USD year
Full Time
About the Company
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Job Description
The Director of Early Precision Medicine Regulatory Affairs leads global regulatory strategy for biomarkers and diagnostics, focusing on early-stage development through proof of concept and supporting registrations.
Requirements
- Drive the development and actively support the execution of innovative, compliant global regulatory strategies
- Serve as the regulatory lead on the Translational Medicine CLIA Laboratory Steering Committee
- Champion innovative regulatory strategies to resolve complex challenges and accelerate patient access
Benefits
- Medical, pharmacy, dental and vision care
- Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP)
- Financial well-being resources and a 401(K)
- Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support
- Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility
- Parental, caregiver, bereavement, and military leave
- Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources
- Other perks like tuition reimbursement and a recognition program