Senior Clinical Theranostic Specialist

We are seeking a Senior Clinical Theranostics Specialist to serve as a senior field-based clinical and technical expert supporting approved and investigational radiopharmaceutical products. This role drives strategic clinical adoption, institutional readiness, and workflow optimization across imaging and treatment centers. This role works cross-functionally with Medical Affairs, Clinical Development, Clinical Operations, and Commercial to translate scientific innovation into safe, compliant, and scalable real-world implementation.

Key Responsibilities

• 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 efforts for approved agents and clinical trials, including product handling, administration, radiation safety, and radiopharmaceutical licensing considerations.
• Deliver high-impact clinical and technical education to ensure safe, effective, and guideline-aligned product utilization.
• Serve as a senior subject matter expert in nuclear medicine and radiopharmaceutical applications, maintaining deep 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, ensuring accurate documentation and full regulatory compliance.
• Generate actionable field insights on diagnostic imaging and radiopharmaceutical trends, institutional barriers, and adoption dynamics, informing launch strategy.
• Provide medical and scientific congress support as requested, in compliance with company policies and industry regulations.
• Ensure adherence to all SOPs and regulatory frameworks, including U.S. Compliance Code of Conduct, OIG Guidance, PhRMA Code, GCP, HIPAA, and applicable FDA regulations.
• Applies AI to improve team execution and decision-making

Qualifications & Experience

• 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.