Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Bristol Myers Squibb

Clinical Theranostic Specialist

Bristol Myers Squibb

. Serve as a senior field-based clinical and technical expert supporting approved and investigational radiopharmaceutical products .

Posted 11/2/2026full-timeRemote • United StatesSeniorLead💰 $134,505 - $162,988 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in nuclear medicine and radiopharmaceutical applications, with a strong focus on clinical education, workflow optimization, and regulatory compliance. Proven ability to build strategic relationships and lead site readiness initiatives in oncology imaging.

Highest-signal resume keywords
Nuclear Medicine ExpertiseRadiopharmaceutical ApplicationsOncology ImagingClinical Education DeliveryRegulatory Compliance

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Radiopharmaceutical ScienceDiagnostic Imaging TrendsSite Education ImplementationWorkflow OptimizationData Translation into Execution Strategies
Soft Skills
Excellent CommunicationPresentation SkillsOrganizational SkillsStrong Executive PresenceRelationship Building
Certifications & Qualifications
Bachelor's DegreeCNMT Preferred
Industry Keywords
Clinical TrialsMedical AffairsClinical OperationsSOP AdherenceFDA RegulationsOIG GuidancePhRMA CodeGCPHIPAAInstitutional Readiness

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Serve as a senior field-based clinical and technical expert supporting approved and investigational radiopharmaceutical products
  • Advance clinical adoption, institutional readiness, and workflow optimization across imaging and treatment centers
  • Partner with Medical Affairs, Clinical Development, Clinical Operations, and Commercial teams
  • Build and sustain strategic relationships with KOLs and institutional stakeholders
  • Lead site readiness and workflow integration for approved agents and clinical trials, including product handling, administration, radiation safety, and licensing considerations
  • Deliver clinical and technical education for safe, effective, and guideline-aligned product utilization
  • Maintain subject-matter expertise in nuclear medicine, radiopharmaceutical applications, imaging techniques, oncology practice patterns, and emerging therapeutic advances
  • Support clinical trial execution through site training and protocol education
  • Respond to unsolicited scientific inquiries with accurate documentation and regulatory compliance
  • Generate field insights on diagnostic imaging and radiopharmaceutical trends, institutional barriers, and adoption dynamics
  • Provide medical and scientific congress support as requested
  • Ensure adherence to SOPs and applicable regulatory frameworks
  • Apply AI to improve team execution and decision-making

Requirements

What you’ll need
  • Bachelor’s degree required
  • CNMT preferred
  • 7+ years of experience in nuclear medicine, radiopharmaceutical clinical applications, oncology imaging, or a related field
  • 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
  • Must comply with U.S. Compliance Code of Conduct, OIG Guidance, PhRMA Code, GCP, HIPAA, and applicable FDA regulations

Benefits

Comp & perks
  • Additional discretionary incentive cash and stock opportunities
  • Wellbeing support
  • Retirement and financial protection benefits
  • Medical, dental, vision, life and disability insurance offerings
  • Flexible Time Off (FTO) without a set accrual limit for eligible U.S.-based exempt employees
  • 11 paid company holidays each year
  • 160 hours of paid vacation annually for eligible new hires
  • 3 optional holidays for eligible employees
  • Paid sick leave
  • Up to two paid volunteer days per year
  • Summer hours flexibility
  • Medical, personal, parental, caregiver, bereavement, and military leaves of absence
  • Annual Global Shutdown between Christmas Day and New Year's Day
  • Reasonable workplace accommodations/adjustments and ongoing support for people with disabilities