Global Medical Affairs Strategy Lead

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb , RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio:

RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals

We are seeking a Global Medical Affairs Strategy Lead to oversee global medical strategy and enrollment for a given program. This important role involves shaping and executing the global medical strategy for our assets and ensuring scientific excellence. The Global Medical Strategy Director will collaborate closely with cross-functional teams, including Research & Development, Commercial, and Corporate Communications. The position will report to the Medical Strategy Disease Area Head.
Key Responsibilities

- Collaborate closely with R&D, Commercial, Access, and Corporate Communications to shape pipeline and portfolio strategies, ensuring alignment of medical plans with portfolio objectives.

- Support launch planning in close partnership with cross-functional medical affairs and commercial brand teams.

- Partner with clinical development teams and study execution teams, providing scientific and medical expertise to support cross-functional deliverables such as trial design strategy and recruitment.

- Accountable for developing the integrated medical evidence plan for early pipeline assets- including therapeutic and diagnostic agents.

- Support medical communication strategy and pull through in publications, congress planning, advisory boards, and KOL engagement.

- Provide medical leadership across the medical matrix team, including medical positioning, field medical engagement, and external education.

- Engage with key external thought leaders, medical organizations, and patient advocacy groups to inform strategy and uphold scientific credibility.

- Mentor and develop medical staff within a matrixed environment.

- Leverages AI to drive program, portfolio, or functional performance through prioritization and scaled adoption

Qualifications & Experience

- MD, DO, PharmD, or PhD (or equivalent scientific or medical training)

- 5-7 years in medical affairs in oncology pharmaceutical/biotech. Experience with radiopharmaceuticals is preferred.

- Proven ability to collaborate with clinical development, corporate communications, and commercial teams to provide medical leadership on organizational objectives

- Demonstrated experience in building and executing a global medical strategy including medical evidence generation, scientific narrative/medical communications

- Proven ability to lead the global cross functional medical matrix team to execute upon the global/US strategy

- Excellent communication and stakeholder management skills with the ability to influence and build credibility with senior leadership and the global scientific community

- Strong analytical and problem-solving abilities with strategic thinking, business acumen, and willingness to roll-up your sleeves to support execution

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You co