Vice President/Executive Director, Medical Affairs

Role Summary

The Vice President/Executive Director, Medical Affairs will lead three key functions—Medical Science Liaisons (MSLs), Patient Advocacy, and Medical Information. This role is central to building Immunome’s external presence, gathering insights to shape strategy, and driving stakeholder engagement across healthcare and patient communities. This is a highly dynamic role: the ideal candidate will be able to roll up their sleeves and do the groundwork while leading the development of evolving functions.

Responsibilities

• National MSL Leadership: Build, train, and lead the MSL team.
• Develop strategic field plans and educational materials.
• Engage healthcare professionals and synthesize external insights.
• Define and track performance metrics.
• Patient Advocacy Leadership: Lead relationships with sarcoma patient advocacy groups (PAGs).
• Develop and execute a strategic engagement plan.
• Bring patient perspectives into internal planning and activities.
• Medical Information Leadership: Oversee medical information systems and response materials.
• Select and manage external partners.
• Ensure proper handling of adverse events and product inquiries.
• Cross-functional Expectations: Stay current on sarcoma research and therapeutic trends.
• Collaborate across departments and represent the patient and HCP voice internally.
• Maintain compliance with industry regulations.
• Manage function-specific budgets and KPIs.

Qualifications

• Advanced scientific degree (PhD, PharmD, MD, or DO).
• 12+ years in Medical Affairs, with oncology experience.
• Proven leadership of field-based teams and product launches.
• Comfortable building and scaling new functions.

Knowledge

• Proven track-record of effective leadership of field teams.
• Experience with product launches, especially in a highly competitive environment.
• Experience working directly within other functions (e.g., Scientific Communication, Operations, Clinical Development) is highly desirable.
• Comprehensive understanding of US regulatory, legal, and compliance guidelines in the pharmaceutical industry, with a commitment to high ethical standards and scientific integrity.
• Excellent communication, presentation, and time and project management skills.

Education

• Not specified in the provided content.

Additional Requirements

• Hybrid role based in Bothell, WA with three in-office days per week.