Radiopharmaceutical Applications Team 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: https://careers.bms.com/rayzebio/

Radiopharmaceutical Applications Team 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: https://careers.bms.com/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 Team Lead for Radiopharmaceutical Clinical Applications to build, lead, and develop the clinical applications team in medical affairs supporting approved and investigational radiopharmaceutical products.   This role combines external scientific engagement, clinical and technical field leadership, and organizational capability building. This leader will partner closely with Medical Affairs, Clinical Development/Operations, Commercial, to support clinical trials, launch readiness, and lifecycle management initiatives, reporting to the Head of Medical Affairs External Engagement.

Key Responsibilities

Team Leadership & Capability Building

• Build, recruit, onboard, and develop a high-performing Radiopharmaceutical Clinical Applications team.
• Provide ongoing mentorship, coaching, and performance management to ensure scientific excellence, field impact, and career development.
• Establish clear operating models, field engagement standards, and performance metrics to drive consistency and scalability.
• Develop training curricula, playbooks, and best practices to support current and future clinical trial activities including study start up, trial execution, and product launches
• Foster a culture of accountability, collaboration, learning agility, and continuous improvement.

External Engagement & Clinical Leadership

• Develop and maintain strategic relationships with Key Opinion Leaders (KOLs) and Healthcare Providers (HCPs), including Nuclear Medicine Physicians, Radiologists, Radiation Oncologists, Technologists, Radiation Safety Officers, Health Physicists, Nursing Staff, and Advanced Practice Providers.
• Position the clinical applications team as trusted scientific and operational partners to imaging centers, treatment sites, and academic institutions.
• Ensure high-quality, consistent delivery of clinical and technical education across the territory.

Clinical & Technical Education

• Oversee and support training programs on product handling, administration, radiation safety, workflow optimization, and regulatory requirements.
• Guide site readiness efforts for onboarding sites/commercialization for approved products and clinical trials, including but not limited to onboarding new sites -including RAM licensing considerations,  equipment calibration, on-site RPT preparation infusion workflows and other radiopharmacy considerations, radiation exposure monitoring and other staff training.
• Maintain deep expertise in nuclear medicine, molecular imaging, oncology practice patterns