NuvalentNU

Director, Medical Affairs Strategy

Nuvalent is a clinical-stage biopharmaceutical company focused on creating precisely targeted therapies for patients with cancer, designed to overcome the limitations of existing therapies for clinically proven kinase targets.

Nuvalent

Employee count: 51-200

United States only

The Company:
With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.

The Role:
Reporting to the Senior Director of Medical Affairs, the Associate Director, Medical Strategy will support the development and execution of Medical Affairs strategy. This role will contribute 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.

Competencies Include:
• 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; 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 also balancing the ability to manage and execute operational details.
• Ability to effectively manage multiple projects with competing priorities.

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 is 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.

• Up to 25% domestic travel.

Nuvalent provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.

Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.

Please be advised that all legitimate correspondence from a Nuvalent employee will come from "@nuvalent.com" email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “[email protected]” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person.

If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.

About the job

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Job type

Full Time

Experience level

Director

Location requirements

Hiring timezones

United States +/- 0 hours

About Nuvalent

Learn more about Nuvalent and their company culture.

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At Nuvalent, Inc., we are at the forefront of oncological innovation, dedicated to creating precisely targeted therapies that address the significant unmet needs of cancer patients. Leveraging our deep expertise in chemistry and state-of-the-art structure-based drug design, we are revolutionizing the development of novel small molecules. Our innovative approach focuses on engineering therapies with exquisite target selectivity, a critical factor in overcoming drug resistance, minimizing adverse events often associated with less targeted treatments, and effectively addressing brain metastases, a common and challenging complication in many cancers. We believe this precision is key to driving more durable and meaningful responses for patients, ultimately transforming their treatment journeys and outcomes.

Our robust pipeline features parallel lead programs targeting ROS1-positive and ALK-positive non-small cell lung cancer (NSCLC), two areas where existing therapies have limitations. Beyond these advanced programs, Nuvalent is actively pursuing multiple discovery-stage research initiatives, continually seeking new clinically proven kinase targets. This relentless pursuit of scientific advancement underscores our commitment to expanding the frontiers of cancer treatment. Our team, comprised of experienced scientists and industry veterans, is driven by a shared passion for patient impact, empowerment, and collaboration. These core values guide our daily work as we strive to translate groundbreaking scientific insights into tangible therapeutic options that can make a profound difference in the lives of those affected by cancer. We are committed to not only advancing our current programs but also to fostering a culture of continuous innovation to tackle the evolving challenges in oncology.

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