Medical Director, US Rare Cardiac, MD

Pfizer • New York City, NY

23h • Hybrid

About The Position

The Medical Director will provide scientific and medical expertise in Transthyretin Amyloid Cardiomyopathy (ATTR-CM) contributing to the development and execution of U.S. medical strategies and tactics for Vyndamax. The role will be an integral member of the U.S. medical affairs organization and cross-functional U.S. Vyndamax team(s). The Medical Director will support key internal and external medical initiatives, including engagement with healthcare professionals, identification of clinical care gaps, and development of customer-focused scientific communication, educational resources, and therapeutic area training(s). The role will work closely with Field Medical, Global Medical Affairs and cross-functional colleagues to support and execute upon the U.S. Medical Affairs plan.

Requirements

• MD/DO professional degrees with 4+ years of experience.
• Knowledge and experience in Heart Failure/ATTR-CM is preferred
• Understanding of the drug development process
• Knowledge of health care economics and its impact on medical decision making
• Strong analytical skills
• Customer-oriented approach with the ability to work effectively in cross-functional and matrix teams
• Proven strategic thinking skills with the ability to interpret and implement strategic directions
• Ability to manage multiple tasks and meet deadlines effectively
• Creativity, resourcefulness, high energy and flexibility
• Professional demeanor with strong interpersonal skills when working with external customers and internal colleagues
• Excellent verbal and written communication skills, including strong presentation skills
• Candidates must be authorized to be employed in the U.S. by any employer.
• U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

Responsibilities

• Supports the development and execution of U.S. medical strategies and tactics in support of Vyndamax
• Collaborates with cross-functional colleagues from commercial, field medical, HEOR, digital, US medical information and relevant internal colleagues to enhance and deliver upon US medical plan(s)
• Serves as a Medical Affairs reviewer within the U.S. Review Committee (RC), supporting scientific accuracy and compliance of promotional and non‑promotional materials in collaboration with Legal, Regulatory, and Marketing colleagues.
• Serves as a reliable scientific resource regarding disease state, clinical data, product labeling, and competitive landscape for ATTR-CM.
• Supports and coordinates U.S. medical congress activities, including coverage planning, session prioritization, and onsite medical support, in alignment with U.S. Medical Affairs plans.
• Provides scientific input into the development of medical and educational content, ensuring accuracy, clinical relevance, and alignment with medical strategy, and incorporating insights from Field Medical and customer interactions, as appropriate
• Supports the customer insights process, collaborating with Field Medical and internal stakeholders to incorporate insights into medical activities and content, and participating in advisory boards or other insight‑generation activities, as appropriate.
• Supports therapeutic area and product training needs by delivering scientific training to new cross‑functional colleagues and supporting training related to new medical content, as appropriate.
• Partners with U.S. Medical Information to provide expert input into Medical Letters and response documents, as needed.

Benefits

• 401(k) plan with Pfizer Matching Contributions
• additional Pfizer Retirement Savings Contribution
• paid vacation
• holiday and personal days
• paid caregiver/parental and medical leave
• health benefits to include medical, prescription drug, dental and vision coverage.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree
• Number of Employees: 5,001-10,000 employees