Radiopharmaceutical Applications Team Lead

Bristol Myers Squibb

1d•Remote

About The Position

At RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, the mission is to develop transformative radiopharmaceutical therapies for cancer patients. The company, headquartered in San Diego, CA, focuses on improving survival by harnessing targeted radioisotopes and developing innovative drugs against solid tumor targets. RayzeBio aims to be a global leader in radiopharmaceuticals, led by an experienced entrepreneurial team. This role is for a Team Lead for Radiopharmaceutical Clinical Applications, responsible for building, leading, and developing a clinical applications team within medical affairs. This team will support approved and investigational radiopharmaceutical products. The position involves external scientific engagement, clinical and technical field leadership, and organizational capability building, partnering closely with Medical Affairs, Clinical Development/Operations, and Commercial teams to support clinical trials, launch readiness, and lifecycle management initiatives. The role reports to the Head of Medical Affairs External Engagement.

Requirements

Bachelor’s degree required.
8+ years of experience in nuclear medicine, radiopharmaceutical clinical applications, oncology imaging, or related field.
Prior experience leading or mentoring field-based clinical or medical teams.
Demonstrated success recruiting, developing, and retaining high-performing talent.
Advanced understanding of radiopharmaceutical science, nuclear medicine workflows, and diagnostic imaging trends.
Proven ability to translate complex scientific data into practical, site-level implementation strategies.
Strong executive presence with the ability to build institutional relationships.
Highly organized with the ability to manage competing priorities in a fast-paced environment.
Approximately 60% travel required.

Nice To Haves

Advanced clinical or scientific degree (CNMT, NP) preferred.
Experience working in both biotech and structured pharma environments preferred.

Responsibilities

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.
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.
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, and emerging radiopharmaceutical innovations.
Support Investigator Sponsored Research (ISRs) and company-sponsored clinical studies aligned with pipeline strategy.
Partner cross-functionally with Clinical Development and Clinical Operations to ensure site preparedness, quality execution, and enrollment support.
Define & promote collaborative ways of working with cross functional field partners to embody a “one team” white glove approach to field engagement.
Ensure appropriate response and documentation of unsolicited scientific inquiries in alignment with regulatory requirements.
Translate field insights into actionable internal strategies.
Provide medical and scientific congress support as requested.
Maintain full compliance with company SOPs, corporate policies, and regulatory frameworks, including U.S. Compliance Code of Conduct, OIG Guidance, PhRMA Code, GCP, HIPAA, and applicable FDA regulations.

Benefits

Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees).
Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays.
Unlimited paid sick time (based on eligibility).
Up to 2 paid volunteer days per year (based on eligibility).
Summer hours flexibility (based on eligibility).
Leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs.
Annual Global Shutdown between Christmas and New Years Day.