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Bristol Myers Squibb

Senior Clinical Theranostic Specialist

Bristol Myers Squibb

. 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 .

Posted 11/10/2026full-timeRemote • United StatesSenior💰 $149,860 - $181,595 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in nuclear medicine and radiopharmaceutical applications, with a strong focus on clinical trial execution, site education, and regulatory compliance. Proven ability to build strategic relationships with key opinion leaders and institutional stakeholders while applying advanced knowledge of imaging techniques and oncology practice patterns.

Highest-signal resume keywords
Nuclear Medicine ExpertiseRadiopharmaceutical ApplicationsClinical Trial ExecutionRegulatory ComplianceOncology Imaging

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Radiopharmaceutical ScienceImaging TechniquesSite Education ImplementationData Translation into StrategiesWorkflow Integration
Soft Skills
Excellent CommunicationPresentation SkillsOrganizational SkillsStrong Executive PresenceRelationship Building
Industry Keywords
Clinical DevelopmentRadiation SafetySOP AdherenceFDA RegulationsOIG GuidancePhRMA CodeGCPHIPAABiotech EnvironmentInstitutional Barriers

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • 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 for safe, effective, and guideline-aligned product utilization
  • Serve as a senior subject matter expert in nuclear medicine and radiopharmaceutical applications
  • Maintain 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 with accurate documentation and regulatory compliance
  • Generate 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
  • 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

Requirements

What you’ll need
  • Bachelor’s degree required
  • 5–7+ 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 strongly preferred

Benefits

Comp & perks
  • Additional discretionary incentive cash and stock opportunities
  • Wellbeing support benefits
  • Retirement and financial protection benefits
  • Medical, dental, vision, life and disability insurance offerings
  • Flexible Time Off (FTO) for U.S.-based exempt employees
  • 11 paid company holidays per year
  • 160 hours of paid vacation annually for new hires for non-exempt employees, RayzeBio employees, and employees located in Puerto Rico
  • 3 optional holidays for non-exempt employees, RayzeBio employees, and employees located in Puerto Rico
  • Paid sick leave, depending on eligibility
  • Up to two paid volunteer days per year, depending on eligibility
  • Summer hours flexibility
  • Leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs
  • Annual Global Shutdown between Christmas Day and New Year's Day for eligible employees
  • Reasonable workplace accommodations/adjustments and ongoing support for people with disabilities