Director, Medical Affairs Strategy

About the Company

Nuvalent is a company with deep expertise in chemistry, focused on creating selective medicines designed to address the needs of patients with cancer. The organization brings together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.

About the Role

The Associate Director, Medical Strategy will report to the Senior Director of Medical Affairs and support the development and execution of Medical Affairs strategy. This role contributes to cross-functional planning and implementation of medical initiatives, including advisory boards, evidence generation, investigator-sponsored research (ISR), and promotional/medical material review. The Associate Director will collaborate closely with Clinical Development, Commercial, Regulatory, and Field Medical teams to ensure strategic alignment and seamless execution.

Responsibilities

• Support development and execution of annual Medical Affairs strategic and tactical plans.
• Collaborate cross-functionally with Clinical, Commercial, Regulatory, and Field Medical to ensure alignment with scientific and business objectives.
• Operationalize and manage Medical Affairs activities such as advisory boards, symposia, scientific congress planning, and educational initiatives.
• Serve as a key Medical Affairs contributor on the Promotional Review Committee (PRC) and Medical Review Committee (MRC) to ensure scientific accuracy, compliance, and alignment with medical strategy.
• Support the planning and implementation of the Investigator-Sponsored Research (ISR) program, including proposal review, coordination of internal evaluations, and communication with investigators.
• Partner with Clinical Development to integrate healthcare provider insights and support the design and execution of clinical trials.
• Collaborate with Commercial colleagues on compliant alignment of strategy and assist with development of promotional materials including slide decks, FAQs, and internal training content.
• Help develop and maintain internal Medical Affairs processes, SOPs, and guidance documents.
• Gather, synthesize, and share scientific and clinical insights from KOL interactions, advisory boards, and scientific conferences.
• Assist in vendor oversight and budget management for assigned initiatives.

Qualifications

• Advanced, medical/scientific doctoral-level degree required: PharmD, PhD, MD (or equivalent).
• 10+ years of experience in the pharmaceutical, biotech, or other relevant industries, including 3+ years in Medical Affairs (preferred).
• Experience contributing to medical strategy with strong operational and executional skills.
• Oncology experience required; solid tumor experience strongly preferred.
• Prior experience supporting advisory boards, PRC/MRC, and ISR programs.
• Experience collaborating across Clinical and Commercial functions.
• Strong project management and scientific communication skills.

Skills

• Demonstrated ability to collaborate across matrixed, cross-functional teams in a fast-paced environment.
• Proven ability to manage multiple projects simultaneously with attention to timelines and detail.
• Strong communication and interpersonal skills; ability to build trust and foster relationships internally and externally.
• Able to work independently, take initiative, and adapt quickly to evolving priorities.
• Recognized leader who exhibits effective communication, emotional intelligence, and influencing skills within a matrix operating environment.
• Demonstration of strategic thinking and high-level planning while balancing operational details.
• Ability to effectively manage multiple projects with competing priorities.

Pay

Annual Salary Range: $230,000—$260,000 USD

Benefits

• Comprehensive medical, dental, and vision insurance.
• 401(k) retirement savings plan.
• Generous paid time off, including a summer and winter company shutdown.

Schedule

• Up to 25% domestic (and possibly international) travel.