Bristol Myers Squibb logo

Associate Director, Global Medical Affairs, US Iberdomide

Bristol Myers Squibb

Madison, NJ; Princeton, NJHybridPosted 1 day ago$166,350 - $201,571/year
Full TimeDirector & AboveMedical AffairsPharmaceutical
Original posting ↗

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.

Job description

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.

Key Responsibilities

US Medical Strategy and Scientific Leadership

  • 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.

Field Medical Partnership & Scientific Exchange

  • 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.

External Engagement & Medical Insights

  • 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.

Evidence Generation & Scientific Communications

  • 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.

Cross-Functional Collaboration

  • 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.

Requirements

  • MD, PharmD, PhD or equivalent
  • 3-5+ years of pharmaceutical industry experience
  • 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

Benefits

  • Wellbeing Support
  • Retirement Benefits
  • Financial Protection Benefits
  • Medical, Dental & Vision
  • Life & Disability Insurance
  • Flexible Time Off
  • 11 Paid Company Holidays
  • Paid Sick Leave
  • Volunteer Days
  • Summer Hours Flexibility
  • Global Shutdown

Company overview

Bristol Myers Squibb is a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. Founded in 1887 and headquartered in Princeton, New Jersey, the company operates with a unique BioPharma strategy that combines the reach and resources of a major pharmaceutical company with the entrepreneurial spirit and agility of a biotech firm. BMS focuses on transformative therapies in key therapeutic areas including oncology, hematology, immunology, cardiovascular disease, and fibrosis. The company has built a sustainable pipeline of potential therapies and leverages translational medicine and data analytics to deliver the right medicine to the right patient at the right time. With over 10,000 employees worldwide, Bristol Myers Squibb maintains a strong commitment to scientific excellence, patient-centric innovation, and global health equity through its foundation. The company's portfolio includes groundbreaking treatments such as Opdivo (nivolumab) for cancer, Eliquis (apixaban) for cardiovascular conditions, and Orencia (abatacept) for autoimmune diseases, among others.

Explore more jobs of your matchFind more biopharma roles with GetBioJob.