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Bristol Myers Squibb

Executive Director, Global Medical Oncology – Iza-Bren Medical Product Lead

Bristol Myers Squibb

. Develop and execute a unified global medical strategy for Izabren across tumor types and lines of therapy .

Posted 11/11/2026full-timePrinceton • New Jersey • United StatesSenior💰 $254,530 - $308,434 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in developing and executing global medical strategies, leading cross-functional teams, and managing stakeholder relationships in the pharmaceutical industry. Proven ability to drive decision-making, optimize trial execution, and deliver measurable outcomes in oncology.

Highest-signal resume keywords
Global Medical Strategy DevelopmentOncology ExperienceCross-Functional LeadershipStakeholder ManagementProject Management

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Medical AffairsClinical DevelopmentRegulatory KnowledgeBudget ManagementKPI MonitoringTrial Execution OptimizationADC ExperienceBispecific AntibodiesPhase 3 Oncology DevelopmentSolid Tumors
Soft Skills
Relationship BuildingChange ManagementCommunication SkillsInfluencing SkillsTeam Leadership
Tools & Technologies
DashboardsReporting Tools
Certifications & Qualifications
MDPhDPharmD
Industry Keywords
PharmaceuticalsInternational MarketsHealthcare DiversityMedical EducationKey Opinion Leaders

About the role

Key responsibilities & impact
  • Develop and execute a unified global medical strategy for Izabren across tumor types and lines of therapy
  • Lead and manage dedicated Global and U.S. Izabren medical teams
  • Drive rapid decision-making and execution across the program
  • Ensure accountability at international, regional, and field levels
  • Optimize trial execution and site engagement across diverse markets
  • Monitor the competitive landscape and adapt strategies
  • Oversee resource allocation, budget management, and strategic prioritization
  • Establish and monitor KPIs, dashboards, and reporting tools
  • Partner with Clinical Development, Safety, Translational/Biomarker, and Regulatory teams
  • Collaborate with SystImmune counterparts on joint medical and scientific alignment
  • Build and empower regional Izabren leads and dedicated MSLs
  • Accelerate site activation, recruitment, and medical education
  • Engage key opinion leaders, investigators, and professional societies
  • Plan data dissemination at key congresses
  • Partner with Global Medical, Development, Commercial, Market Access, and Patient Advocacy teams
  • Represent Izabren in stakeholder, partnership, and joint governance meetings

Requirements

What you’ll need
  • Advanced degree in medicine, science, or related field (MD, PhD, PharmD; MD preferred)
  • 15+ years of medical affairs, development, or commercial experience
  • Strong track record in international markets
  • Pharmaceutical experience in solid tumors, including breast, thoracic, GI and GU cancers
  • Experience with ADCs, bispecific antibodies and/or Phase 3 oncology development strongly preferred
  • Proven expertise leading large, geographically distributed teams
  • Deep understanding of regulatory, healthcare, and cultural diversity across international markets
  • Demonstrated ability to execute strategies delivering measurable business and patient outcomes
  • Strong cross-functional leadership and stakeholder management skills
  • Ability to collaborate effectively across R&D, disease management, marketing, and external development
  • Strong external relationship-building skills
  • Outstanding project management and change management capabilities
  • Experience leading teams through market or organizational transformation
  • Ability to communicate and influence decisions with senior leadership and matrix teams

Benefits

Comp & perks
  • Additional discretionary incentive cash and stock opportunities
  • Wellbeing support
  • Retirement and financial protection benefits
  • Medical, dental, vision, life and disability insurance offerings
  • Flexible Time Off (FTO) without a set accrual limit for eligible U.S.-based exempt employees
  • 11 paid company holidays each year
  • 160 hours of paid vacation annually for eligible new hires
  • 3 optional holidays for eligible non-exempt, RayzeBio and Puerto Rico employees
  • Paid sick leave, where eligible
  • Up to two paid volunteer days per year
  • Summer hours flexibility
  • Leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs
  • Annual Global Shutdown between Christmas Day and New Year's Day for eligible employees
  • Reasonable workplace accommodations/adjustments and ongoing support
  • Flexible work models