Director, Global Medical Cardiovascular, Mavacamten

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The Director Global Medical Cardiovascular Mavacamten is a key medical leader responsible for shaping and executing both Worldwide and US medical strategy for mavacamten across its lifecycle in hypertrophic cardiomyopathy (HCM). This role provides scientific and clinical leadership across global and US medical initiatives including medical strategy development evidence planning publications congress strategy medical education external communications and crossfunctional scientific engagement.

The Director leads in a highly collaborative environment with a diverse matrix team. The Director partners closely with Regional Market Medical Medical Communications Clinical Development Regulatory Safety Market Access Marketing and Commercial teams requiring strong crossfunctional leadership to ensure medical strategies are aligned scientifically rigorous clinically meaningful and responsive to the evolving HCM landscape.

Key Responsibilities

• Lead development and execution of integrated Worldwide and US medical strategies for mavacamten across indications and lifecycle stages

• Partner closely with Medical Market Leads to translate global medical strategy into region - specific medical plans detailing clear executional priorities

• Drive alignment across crossfunctional stakeholders to ensure medical strategy informs and is informed by development regulatory access and commercialization considerations

• Serve as a global and US medical subject matter expert in hypertrophic cardiomyopathy

• Provide leadership for global and US content generation strategy disease education strategy and data interpretation

• Act as a trusted crossfunctional medical advisor providing clear scientific guidance and clinical context to internal stakeholders

• Contribute to Worldwide and US evidence planning including RWE Phase 4 studies registries and investigatorsponsored research as needed

• Support global and US publication and content strategy including review of abstracts manuscripts congress materials and externally-facing resources. Participate in medical review processes for promotional and nonpromotional materials as required

• Provide medical leadership for global and US congress strategy and execution

• Partner with Global US and regional medical teams to establish and maintain long-term Thought Leader Engagement Strategy. Manages Global Thought Leader activities including Advisory Boards - aligns with functionsmarketsand regions to ensure transparencyregardingTL activities

• Coordinate with crossfunctional partners to ensure scientific engagement strategies are aligned and appropriately governed

• Act as a core member of the WorldwideUS mavacamten medical and commercialization matrix teams

• Demonstrate strong crossfunctional leadership in a highly matrixed environment influencing without authority and driving alignment across Medical Clinical Development Regulatory Safety Market Access Marketing and Commercial teams

• Support medical training initiatives and ensure consistency of scientific messaging across Global and US teams

• Ensure all Worldwide and US medical activities comply with company policies and medical governance standards

Qualifications & Experience

• Advanced scientific degree (MD PhD PharmD PA/NP)

• At least 5-10 years of experience in Medical Affairs within pharmaceutical or biotech with increasing responsibility

• Experience supporting both global and US medical strategy strongly preferred

• Cardiovascular disease expertise required; HCM or rare disease experience strongly preferred

• Demonstrated success partnering crossfunctionally in complex matrixed organizations

• Prior industry experience inCVMedicalaffairs/Medical StrategyProduct launch andClinical Research or related experience is preferred.

• Must have experience working inmulti-functional project team and managing external agencies.

• Proven ability to plan and implement medical congresses and advisory boards.

• Familiarity with all phases of drug development is desirable

Skills & Competencies

• Strong scientific and clinical acumen with the ability to translate data into actionable medical strategy

• Ability to work effectively with cross functional teams including clinical commercialization regulatory and early discovery.

• The successful candidate must be highly professional with excellentrelationship-buildingand communication skills including the ability to articulate both verbally and in writing complex scientific principles.

• Ability to navigate ambiguity and align diverse stakeholders around shared medical objectives

• Acts with the highest level ofleadership with Enterprise Mindsetand flexibility

• Attention to detail with excellent planning timemanagementand organizational skills

• Resiliency and strong adaptability to change

• High-level negotiationskillsand the ability to resolve conflict in a constructive manner

• Innovative and entrepreneurial thinking

• Functions with excellent judgment high integrity and in compliance with all lawsregulationsand policies

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If you come across a role that intrigues you but doesnt 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.

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 employees 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 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.

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On-site Protocol

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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 . Visit 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: Protection

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