Radiopharmaceuticals Applications Liaison

About the role

RayzeBio, a Bristol Myers Squibb company headquartered in San Diego, California, is a biotechnology company focused on improving cancer survival through targeted radioisotopes. The company is developing innovative therapies for solid tumor targets and aims to become a global leader in radiopharmaceuticals. We are seeking a Radiopharmaceutical Applications Liaison to serve as a senior field-based clinical and technical expert supporting approved and investigational radiopharmaceutical products.

Responsibilities

• Build and sustain strategic relationships with KOLs and institutional stakeholders, including Nuclear Medicine Physicians, Radiologists, Radiation Oncologists, Technologists, Radiation Safety Officers, Health Physicists, Nursing Staff, and Advanced Practice Providers.
• Lead site readiness and workflow integration efforts for approved agents and clinical trials, including product handling, administration, radiation safety, and radiopharmaceutical licensing considerations.
• Deliver high-impact clinical and technical education to ensure safe, effective, and guideline-aligned product utilization.
• Serve as a senior subject matter expert in nuclear medicine and radiopharmaceutical applications, maintaining deep expertise in imaging techniques, oncology practice patterns, and emerging therapeutic advances.
• Support clinical trial execution through site training, protocol education, and alignment with Clinical Development and Operations.
• Respond to unsolicited scientific inquiries regarding approved and investigational products, ensuring accurate documentation and full regulatory compliance.
• Generate actionable field insights on diagnostic imaging and radiopharmaceutical trends, institutional barriers, and adoption dynamics, informing launch strategy.
• Provide medical and scientific congress support as requested, in compliance with company policies and industry regulations.
• Ensure adherence to all SOPs and regulatory frameworks, including U.S. Compliance Code of Conduct, OIG Guidance, PhRMA Code, GCP, HIPAA, and applicable FDA regulations.
• Apply AI to improve team execution and decision-making.

Qualifications & Experience

• Bachelor’s degree required. (CNMT preferred)
• 7+ years of experience in nuclear medicine, radiopharmaceutical clinical applications, oncology imaging, or related field.
• Demonstrated experience leading complex site education and workflow implementation initiatives.
• Advanced understanding of radiopharmaceutical science, nuclear medicine operations, and diagnostic imaging trends.
• Ability to translate complex data into practical, site-level execution strategies.
• Strong executive presence and ability to build institutional relationships.
• Experience working cross-functionally within a matrixed biotech or pharmaceutical environment.
• Excellent communication, presentation, and organizational skills.
• Experience in oncology and radiopharmaceuticals is strongly preferred.