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This position plays a critical role in the development and execution of BMS' WW & US medical strategy for a next-generation cardiac myosin inhibitor within the cardiovascular portfolio. The MedicalMedicalProduct Lead (MPL) is a strategic leader with broad responsibilities across theMedicalorganization and a key leader of the cross-functional matrix, providing medical insights and interpretation of the evolvingheart failure(HF)and cardiomyopathylandscape and translating emerging clinical and scientific data across the organization. The MPL has overall accountability to develop aligned medical strategies and execute core medical deliverables, including Integrated Evidence Plans, Scientific Narratives, and External Engagement and Advocacy plans as the lead of the cross-functional Asset/Indication Medical Strategy (AIMS) team.
The Director,MPLwill provide strategic oversight fora newasset inheart failure andcardiomyopathy, initially focused onheart failure with preserved ejection fraction (HFpEF)and future life cycle management opportunities. This leader will direct and navigate complex issues across a broad cross-functional matrix to ensure optimal medical affairs strategy is developed and executed, including clear differentiation,evidence strategies that address monitoring burden and safety margin, and internal positioning across the broadermyosininhibitor franchise. This medical leader will report to the VP,HeadofCardiovascularMedical Affairsand work closely with CV global program leadsin Clinical Development.
Shape and articulate a clear scientific differentiation narrative versus existing and emerging myosin inhibitorsand modulators, including considerations related to pharmacokinetics, pharmacodynamics, titration,monitoringburden, safety margin, and physician confidence.
Partner across Worldwide Medical, Development, Regulatory, Commercial, HEOR, and Access to ensurethe assetis positioned appropriately within the BMS cardiovascular portfolio and that internal sequencing and franchise strategy are clearly defined.
Develop and execute global medical strategy, scientific narratives, and insight plans that reflect the evolving treatment landscape, including competitive dynamics and emerging standards of care.This will be put in the context of the broader CV BMS cardiomyopathy franchise, with expected collaborations across theother assetteams.
Lead workstreams toidentifyevidence gaps and develop comprehensive Integrated Evidence Plans (IEPs), including strategies to assess clinically meaningful differentiation such as usability in practice,monitoringrequirements, and safetyprofile.
Deliver WW & US Medical Communications plans, including global publications strategy, scientific exchange, symposia, and data dissemination at key cardiovascular congresses.
Contribute to shaping competitive and access strategies by providing the global medical perspective on target product profile, value drivers, external stakeholder needs, and future life cycle expansion opportunities.
Qualifications & Experience
Minimum of 8+ years working in the pharmaceutical industry in Medical Affairs, Medical Strategy, or Clinical Research, with experience in cardiovascular medicine preferred.
Experience supporting asset strategy in early- to mid-stage development, including medical input into differentiation, evidence planning, and life cycle strategy, is preferred.
The successful candidate should have strong analytical skills, strong scientific data and evidence interpretation and contextualization, and the ability to work effectively with cross-functional teams including clinical, commercialization, regulatory, HEOR, and Access.
Excellent strategy development, critical thinking, decision making, anddemonstratedability to successfully create and implement both short- and long-range global medical plans.
Ability toanticipateneeds and assess scientific, business, and organizational risks in a complex global environment, including risks related to competitive positioning, internal franchise dynamics, and external adoption barriers.
Must be familiar with all phases of drug development, including clinical development, regulatory strategy, and life cycle management in a global context.
If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Princeton - NJ - US: $207,490 - $251,433 

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work-life benefits include:
Paid Time Off
US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
Supporting People with Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Candidate Rights
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
R1605170 : Director, Global Medical Cardiovascular, Medical Product Lead
