Clinical Theranostic Specialist

Bristol Myers Squibb

9d • $134,505 - $162,988 • Remote

About The Position

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, is seeking a senior field-based clinical and technical expert to support approved and investigational radiopharmaceutical products. The specialist advances clinical adoption, institutional readiness, and workflow optimization across imaging and treatment centers. The role partners with Medical Affairs, Clinical Development, Clinical Operations, and Commercial teams to translate scientific innovation into safe, compliant, and scalable real-world practice.

The position involves building relationships with clinical and institutional stakeholders, leading site readiness and workflow integration, delivering clinical and technical education, supporting clinical trial execution, responding to unsolicited scientific inquiries, and generating field insights. The specialist maintains expertise in nuclear medicine, imaging techniques, oncology practice patterns, and emerging therapeutic advances, while ensuring compliance with applicable company policies, codes, SOPs, and regulatory requirements. The role also applies AI to improve team execution and decision-making.

The position is remote within the United States. The listed starting salary range is $134,505–$162,988 for full-time employees. Employees may also be eligible for discretionary cash incentives and stock opportunities. Benefits may include wellbeing support, retirement and financial protection benefits, insurance, paid time off, paid holidays, volunteer days, and leave benefits, subject to eligibility and applicable plan terms.

Requirements

• Bachelor’s degree required.
• At least 7 years of experience in nuclear medicine, radiopharmaceutical clinical applications, oncology imaging, or a 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.

Nice To Haves

• CNMT preferred.
• Experience in oncology and radiopharmaceuticals is strongly preferred.

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 for approved agents and clinical trials, including product handling, administration, radiation safety, and radiopharmaceutical licensing considerations.
• Deliver clinical and technical education to support safe, effective, and guideline-aligned product utilization.
• Serve as a senior subject matter expert in nuclear medicine and radiopharmaceutical applications, maintaining 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 about approved and investigational products, ensuring accurate documentation and regulatory compliance.
• Generate actionable field insights on diagnostic imaging and radiopharmaceutical trends, institutional barriers, and adoption dynamics to inform launch strategy.
• Provide medical and scientific congress support as requested, in compliance with company policies and industry regulations.
• Ensure adherence to SOPs and regulatory frameworks, including the 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.

Benefits

• Wellbeing support.
• Retirement and financial protection benefits.
• Medical, dental, vision, life, and disability insurance offerings.
• Eligible U.S.-based exempt employees receive Flexible Time Off without a set accrual limit, subject to manager approval.
• Paid company holidays: 11 per year.
• RayzeBio employees and non-exempt employees receive 160 hours of paid vacation annually for new hires, subject to manager approval, and 3 optional holidays.
• Depending on eligibility, paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs.
• Eligible employees receive an annual Global Shutdown between Christmas Day and New Year's Day.
• Potential eligibility for discretionary incentive cash and stock opportunities.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior