Associate Director, Regulatory Excellence ICVN

Role: Associate Director, Regulatory Excellence within Bristol Myers Squibb's GRS ICV & Neuroscience, serving as a strategic business partner to leadership, overseeing operational planning, compliance, and regulatory initiatives. Responsibilities: lead development of senior leadership presentations, manage regulatory portfolio tracking, coordinate cross-functional information, drive process improvements in regulatory operations, and support organizational and team effectiveness. Collaborate with Clinical Development, CMC, Medical Affairs, and other functions to ensure alignment on regulatory milestones and initiatives. Requirements: Bachelor's in Life Sciences or related field; 7-10+ years in biopharma regulatory or operations roles, with experience managing cross-functional projects in a matrixed environment, preferably with exposure to global regulatory submissions and digital tools. Preferred: experience supporting senior leaders, familiarity with portfolio management and process improvement methodologies, and knowledge of global regulatory processes. HighValue: focus on regulatory excellence in Neuroscience/ICV, leadership support, process optimization, cross-functional coordination, and digital adoption. WorkSetup: role specifics not detailed; likely hybrid or remote based on company policies.