Clinical Theranostic Specialist
Bristol Myers Squibb
August 17, 2026
Remote friendly (Lawrence, NJ)
United States
Medical Affairs
Key Responsibilities
- Build and sustain strategic relationships with KOLs and institutional stakeholders (e.g., Nuclear Medicine Physicians, Radiologists, Radiation Oncologists, Technologists, Radiation Safety Officers, Health Physicists, Nursing, APPs).
- Lead site readiness and workflow integration for approved agents and clinical trials (product handling/administration, radiation safety, licensing considerations).
- Deliver clinical and technical education to support safe, effective, guideline-aligned product use.
- Serve as a senior subject matter expert in nuclear medicine and radiopharmaceutical applications (imaging techniques, oncology practice patterns, emerging therapies).
- Support clinical trial execution via site training and protocol education.
- Respond to scientific inquiries about approved/investigational products with accurate documentation and regulatory compliance.
- Provide field insights on imaging/radiopharmaceutical trends and adoption barriers to inform launch strategy.
- Support medical/scientific congress activities as requested.
- Ensure adherence to SOPs and applicable frameworks (GCP, HIPAA, FDA regulations).
- Apply AI to improve execution and decision-making.
Qualifications & Experience
- Bachelor’s degree required (CNMT preferred).
- 7+ years’ experience in nuclear medicine/radiopharmaceutical clinical applications/oncology imaging or related field.
- Experience leading complex site education and workflow implementation.
- Advanced knowledge of radiopharmaceutical science, nuclear medicine operations, and diagnostic imaging trends.
- Ability to translate complex data into site-level execution strategies.
- Strong executive presence; excellent communication/presentation/organizational skills.
- Cross-functional experience in matrixed biotech/pharma.
- Oncology and radiopharmaceutical experience strongly preferred.
Benefits (highlights)
- Health coverage (medical, pharmacy, dental, vision), wellbeing programs, 401(k), disability and life insurance.
- Paid time off: flexible time off (with manager approval) for US exempt employees; plus vacation/holidays for certain other employee groups.
Encouragement to Apply
- If you’re interested but don’t perfectly match, you’re encouraged to apply anyway.
- Build and sustain strategic relationships with KOLs and institutional stakeholders (e.g., Nuclear Medicine Physicians, Radiologists, Radiation Oncologists, Technologists, Radiation Safety Officers, Health Physicists, Nursing, APPs).
- Lead site readiness and workflow integration for approved agents and clinical trials (product handling/administration, radiation safety, licensing considerations).
- Deliver clinical and technical education to support safe, effective, guideline-aligned product use.
- Serve as a senior subject matter expert in nuclear medicine and radiopharmaceutical applications (imaging techniques, oncology practice patterns, emerging therapies).
- Support clinical trial execution via site training and protocol education.
- Respond to scientific inquiries about approved/investigational products with accurate documentation and regulatory compliance.
- Provide field insights on imaging/radiopharmaceutical trends and adoption barriers to inform launch strategy.
- Support medical/scientific congress activities as requested.
- Ensure adherence to SOPs and applicable frameworks (GCP, HIPAA, FDA regulations).
- Apply AI to improve execution and decision-making.
Qualifications & Experience
- Bachelor’s degree required (CNMT preferred).
- 7+ years’ experience in nuclear medicine/radiopharmaceutical clinical applications/oncology imaging or related field.
- Experience leading complex site education and workflow implementation.
- Advanced knowledge of radiopharmaceutical science, nuclear medicine operations, and diagnostic imaging trends.
- Ability to translate complex data into site-level execution strategies.
- Strong executive presence; excellent communication/presentation/organizational skills.
- Cross-functional experience in matrixed biotech/pharma.
- Oncology and radiopharmaceutical experience strongly preferred.
Benefits (highlights)
- Health coverage (medical, pharmacy, dental, vision), wellbeing programs, 401(k), disability and life insurance.
- Paid time off: flexible time off (with manager approval) for US exempt employees; plus vacation/holidays for certain other employee groups.
Encouragement to Apply
- If you’re interested but don’t perfectly match, you’re encouraged to apply anyway.