Associate Director, Regulatory Excellence & Hematology/Oncology Operations
Bristol Myers SquibbPrinceton, NJ · full time · Director
$173,350 – $210,058
Listed on Bristol Myers Squibb’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role leads regulatory operations and business management for Bristol Myers Squibb's Oncology/Hematology division, supporting a 45-person team and senior leadership across strategic planning, compliance, and portfolio coordination. It suits someone with 7–10 years of biopharmaceutical operations experience who can manage complex cross-functional initiatives and drive process improvement in a matrixed environment.
Our summary, not Bristol Myers Squibb’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- Bachelor's degree in Life Sciences, Pharmacy, or related field
- 7–10 years of experience in business operations, program/project management, regulatory operations, or related roles in biopharmaceutical or healthcare environments
- Demonstrated ability to lead complex projects, develop plans, lead meetings, and deliver outcomes with independence in fast-paced, matrixed environment
- Strong written and verbal communication skills
- Proficiency in Microsoft Office Suite (PowerPoint, Excel, Word, Teams)
Nice to have
- Advanced degree (MSc, PhD, PharmD)
- Experience supporting senior leaders or working in business operations or chief of staff capacity
- Experience in pharmaceutical, biotechnology, or healthcare environments
- Familiarity with portfolio management, resource planning, or operational analytics
- Experience with tools such as SharePoint, Planisware, Veeva, or similar platforms
- Experience with global regulatory submissions (NDAs, BLAs, MAAs or equivalent) and health authority interactions
- Exposure to process improvement methodologies (e.g., Lean, Six Sigma)