Clinical Theranostic Specialist

We need to output HTML fragment with sections: headings

for sections like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections that have real specific content. Must not repeat job title as heading. Must not include Job ID/requisition numbers as headings; can fold minor metadata into short

or drop it. Must preserve all substantive info; remove boilerplate, navigation, legal, EEO, equal-opportunity, scam-warning, duplicated lines, application instructions. Must not create sections with filler like "commensurate with experience". Must not create Pay/Schedule/Benefits unless posting actually states them. The posting includes compensation overview: Remote - United States - US: $134,505 - $162,988. Also mentions benefits: list of benefits. So we can include Pay section with that range. Benefits section with list. Schedule? Not mentioned; remote but no schedule specifics. So we omit Schedule. We need sections: About the role (maybe from description), Responsibilities (Key Responsibilities), Qualifications (Qualifications & Experience), Skills (maybe from qualifications includes skills), Benefits, Pay. We must not repeat job title as heading. Use

for each section heading. We need to preserve all substantive information: need to include details about role, responsibilities list, qualifications list, benefits list, pay range. We must remove duplicated lines, boilerplate like "Learn more about RayzeBio: https://careers.bms.com/rayzebio/" repeated many times, also repeated paragraphs about mission etc. We'll keep one concise version. We must not include application instructions like "If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway." That's application encouragement; maybe considered boilerplate? It's not strictly legal but it's encouraging to apply; might be considered application instruction. Safer to remove. Also remove EEO, disability, data protection, fraud protection, etc. We must keep compensation overview and benefits. We need to format lists with

• . Let's extract substantive content: About the role / overview: "At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on patients." Also later: "RayzeBio, a Bristol Myers Squibb company headquartered in San Diego, California, is a biotechnology company focused on improving cancer survival through targeted radioisotopes. The company is developing innovative therapies for solid tumor targets and aims to become a global leader in radiopharmaceuticals. We are seeking a Clinical Theranostic Specialist to serve as a senior field-based clinical and technical expert supporting approved and investigational radiopharmaceutical products. In this role, you will advance clinical adoption, institutional readiness, and workflow optimization across imaging and treatment centers. You will also partner cross-functionally with Medical Affairs, Clinical Development, Clinical Operations, and Commercial teams to translate scientific innovation into safe, compliant, and scalable real-world practice." We can combine. Responsibilities list (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. (CNMT preferred) - 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 is strongly preferred. Skills could be extracted from qualifications: but we can have a Skills section summarizing: strong communication, presentation, organizational, executive presence, cross-functional collaboration, data translation, etc. However we must not invent; we can list those as skills if they appear. They appear in qualifications. Could make a Skills section with those items. But we already have Qualifications & Experience; maybe we can combine qualifications and skills into one section? The instruction says use headings for sections like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We can include both Qualifications and Skills if content exists. We have qualifications list; skills could be subset: "Excellent communication, presentation, and organizational skills", "Strong executive presence", "Ability to translate complex data", etc. We'll create Skills section with those. Benefits: list from posting: - Health Coverage: Medical, pharmacy, dental, and vision care. - Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP). - Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. - Work-life Benefits Include: Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown. Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program. That's a lot; we need to preserve all substantive information. We'll include as list items maybe summarizing each bullet but keep details. Pay: Compensation Overview: Remote - United States - US: $134,505 - $162,988. Also mention additional incentive cash and stock opportunities (based on eligibility) may be available. Starting compensation range for full-time employee. Final individual compensation decided based on demonstrated experience. Eligibility for specific benefits may vary based on job and location. We'll include that. We must not create Schedule section. Now produce HTML fragment. We need to ensure no stray text outside tags. Use

  headings. Let's craft:

  About the role

  At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on patients. RayzeBio, a Bristol Myers Squibb company headquartered in San Diego, California, is focused on improving cancer survival through targeted radioisotopes, developing innovative therapies for solid tumor targets and aiming to become a global leader in radiopharmaceuticals. As a Clinical Theranostic Specialist, you will serve as a senior field-based clinical and technical expert supporting approved and investigational radiopharmaceutical products, advancing clinical adoption, institutional readiness, and workflow optimization across imaging and treatment centers while partnering cross-functionally with Medical Affairs, Clinical Development, Clinical Operations, and Commercial teams.

  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

  • Bachelor’s degree required. (CNMT preferred)
  • 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 radioph