Associate Director, Global Medical Affairs, US Iberdomide

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. Position Summary The Associate Director, US Iberdomide will be a key scientific and strategic contributor to the Global Medical Affairs team supporting iberdomide for the treatment of multiple myeloma. Reporting to the Director, US Iberdomide, this role will support the development and execution of global medical strategy across the asset lifecycle, with a strong emphasis on scientific engagement, field partnership, and insight generation. The Associate Director will collaborate closely across the matrix to ensure high-quality scientific exchange and effective execution of medical priorities. Key Responsibilities Support development and execution of the US medical strategy for iberdomide, aligned with global guidance and US-specific medical needs. Contribute to the articulation of the US scientific narrative, including unmet need, mechanism of action, and interpretation of emerging clinical data in multiple myeloma. Serve as a scientific expert on iberdomide clinical data, including efficacy, safety, MRD, and translational insights. Partner with the Director, US Iberdomide to ensure medical priorities are aligned with evolving clinical, regulatory, and scientific milestones. Serve as a close partner to US Field Medical (MSLs) by supporting scientific training, field engagement strategy, and responses to complex scientific inquiries. Provide scientific guidance and content support for field-facing materials and internal medical training. Synthesize field insights to inform US medical strategy, data needs, and external engagement priorities. Engage with US-based key opinion leaders, investigators, and community hematology/oncology experts to understand evolving treatment paradigms and scientific needs. Support planning and execution of US advisory boards, steering committees, and scientific exchange meetings. Capture and communicate actionable medical insights internally to inform strategy, publications, and evidence planning. Support US-focused evidence generation, including post-hoc analyses aligned to US medical priorities. Partner with Medical Communications to support US publication planning, abstract development, manuscripts, and congress deliverables. Provide scientific input into US congress strategy. Partner compliantly with Commercial, Regulatory, and Market Access colleagues to ensure aligned scientific understanding across functions. Collaborate closely with Clinical Development and Translational Medicine to ensure US medical insights are integrated into data generation and interpretation. Work with Global counterparts to ensure appropriate alignment while maintaining clear focus on US execution. Qualifications & Experience MD, PharmD, PhD or equivalent. 3-5+ years of pharmaceutical industry experience, with hematology/oncology experience strongly preferred. Demonstrated ability to interpret and clearly communicate complex clinical and scientific data. Experience partnering with US Field Medical teams and engaging US-based external experts. Strong written and verbal communication skills, with experience in scientific presentations. Proven ability to collaborate cross-functionally within a matrixed organization and manage multiple competing priorities. Comfort operating in ambiguity and adapting to emerging data. Ability to travel as needed. Compensation Overview Madison - Giralda - NJ - US: $166,350 - $201,571 Princeton - NJ - US: $166,350 - $201,571 Benefits Subject to the t

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