
Job Overview
Location
Remote - United States - US
Job Type
Full-time
Category
Sales
Date Posted
May 15, 2026
Full Job Description
đź“‹ Description
- • Serve as a senior field-based clinical and technical expert supporting approved and investigational radiopharmaceutical products across imaging and treatment centers in the United States.
- • Build and sustain strategic relationships with key opinion leaders 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 initiatives for radiopharmaceutical therapies, addressing product handling, administration protocols, radiation safety protocols, and radiopharmaceutical licensing requirements.
- • Deliver high-impact clinical and technical education to ensure safe, effective, and guideline-aligned utilization of radiopharmaceutical agents in real-world settings.
- • Act as a subject matter expert in nuclear medicine and radiopharmaceutical applications, maintaining current knowledge of imaging techniques, oncology practice patterns, and emerging therapeutic advances.
- • Support clinical trial execution by providing site training, protocol education, and alignment with Clinical Development and Clinical Operations teams.
- • Respond to unsolicited scientific inquiries regarding approved and investigational products with full compliance to regulatory standards and accurate documentation.
- • Gather and translate field insights on diagnostic imaging trends, institutional adoption barriers, and real-world utilization dynamics to inform launch strategies and product development.
- • Provide medical and scientific congress support in strict adherence to company policies and industry regulations including PhRMA Code, GCP, HIPAA, and FDA guidelines.
- • Ensure full compliance with all standard operating procedures (SOPs) and regulatory frameworks, including the U.S. Compliance Code of Conduct and OIG Guidance.
- • Apply AI tools to enhance team execution and improve decision-making processes in clinical support and field operations.
- • Collaborate cross-functionally with Medical Affairs, Commercial, and Clinical Operations teams to translate scientific innovation into scalable, compliant, and practical clinical workflows.
- • Maintain deep expertise in radiopharmaceutical science, nuclear medicine operations, and oncology imaging to serve as a trusted advisor to healthcare institutions.
- • Work remotely across the United States with frequent travel to institutional sites for training, site visits, and stakeholder engagement.
- • Ensure all field activities align with Bristol Myers Squibb’s global compliance, ethics, and data privacy standards.
Skills & Technologies
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About Bristol-Myers Squibb Company
Bristol-Myers Squibb is a global biopharmaceutical company headquartered in New York City. It discovers, develops, manufactures and markets medicines for cancer, cardiovascular, immunologic, fibrotic and infectious diseases. Formed through the 1989 merger of Bristol-Myers and Squibb, the company has pioneered therapies such as Opdivo, Yervoy and Eliquis. Operating in more than 60 countries, it invests heavily in R&D and partnerships to advance precision oncology, cell therapy and immunotherapy. BMS acquired Celgene in 2019, expanding its oncology and hematology portfolio. The company is committed to sustainability, access to medicines and global health equity initiatives.
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