Associate Director, Regulatory Excellence ICVN

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Summary Bristol Myers Squibb is seeking an Associate Director, Regulatory Excellence, ICVN to lead business management activities within the GRS ICV & Neuroscience organizations. This role serves as a strategic partner to leadership, driving execution of portfolio priorities, operational planning, compliance, and regulatory excellence initiatives. The successful candidate will be recognized internally as a subject matter expert in business operations, exercising considerable latitude in shaping deliverables, leading initiatives of strategic importance, and developing solutions to highly complex, sometimes novel problems with broad impact across the department. The role requires anticipating business and industry trends, representing BMS with key internal and external partners, and ensuring effective planning, meeting leadership, and compliant execution across a matrixed environment.

Operational & Leadership Support Serve as a strategic operational partner to the Therapy Areas VPs, leading development of leadership presentations, business reviews, team communications, and strategic planning materials that inform department priorities and decision-making Develop operational plans and lead the management cadence for the ICVN Regulatory teams, including key leadership meetings, portfolio reviews, and planning cycles, ensuring alignment, follow-through, and compliance with governance expectations Lead follow-up on action items, critical deliverables, and leadership commitments, independently resolving or escalating highly complex issues and developing new options to address risks with broad impact on the department Lead preparation of governance materials, executive briefings, and decision-ready content for senior leadership and cross-functional forums, exercising considerable latitude in determining objectives, framing recommendations, and shaping deliverables Actively identifies organizational risks to the Therapy Area VPs in a timely manner and leads mitigation · Regulatory Portfolio Coordination & Tracking Coordinate cross-team information gathering to support portfolio reviews, resource discussions, and pipeline updates Partner with Regulatory Team Leaders and program teams to monitor and communicate key regulatory milestones, flagging risks or delays proactively Support resource tracking and workload monitoring across the ICVN Regulatory groups to assist leadership in allocation decisions Liaise with Global Regulatory Strategic Operations and project management teams to ensure alignment on submission timelines and deliverables · Regulatory Excellence & Process Improvement Lead the Regulatory Excellence agenda for the ICVN TAs by driving process improvement initiatives of strategic importance, establishing implementation plans, and ensuring progress is measured, communicated, and sustained Identify systemic workflow inefficiencies and develop new approaches to solve highly complex, sometimes novel operational problems that affect team performance, submission quality, and departmental effectiveness Help develop, update, and communicate standard operating procedures (SOPs), work instructions, and best practice guides relevant to ICVN regulatory operations Coordinate training and onboarding activities for new team members, ensuring smooth integration into team processes, systems, and culture Support adoption of new regulatory tools and digital