Associate Director, Regulatory Excellence & Hematology/Oncology Operations

Role: Associate Director of Regulatory Excellence & Hematology/Oncology Operations at Bristol Myers Squibb, overseeing operational and business management activities within the Oncology/Hematology sector. Responsibilities include strategic partnership with leadership, developing operational plans, managing portfolio tracking, driving regulatory process improvements, and ensuring compliance across a team of ~45 professionals. The role involves preparing leadership materials, monitoring regulatory milestones, supporting digital tool adoption, and fostering cross-functional collaboration across Clinical Development, CMC, Medical Affairs, and other functions. Qualifications: Bachelor's in Life Sciences, Pharmacy, or related; 7–10 years in regulatory operations, program management, or biopharma business operations; strong project leadership, communication, and stakeholder management skills; proficiency in MS Office. Preferred: experience supporting senior leaders, knowledge of global regulatory submissions (NDAs, BLAs, etc.), familiarity with portfolio management or process improvement methodologies (e.g., Lean, Six Sigma), and experience with platforms like Veeva or SharePoint. High-value specifics include focus on Hematology/Oncology, regulatory excellence, and managing complex, strategic initiatives in a matrixed environment. The position is hybrid in Princeton, NJ, with leadership in regulatory and cross-functional strategic planning.