Clinical Theranostic Specialist

atBristol Myers SquibbRemoteUS flagUnited StatesFull-timeUncategorizedSeniorLead$134.5k – $163k/year

Posted 1 day ago

This is a fully remote position, open to applicants in United States.

📋 Description

• Act as a senior clinical and technical expert in the field, providing support for both approved and investigational radiopharmaceutical products.

• Facilitate the clinical adoption, institutional preparedness, and workflow enhancements at imaging and treatment facilities.

• Collaborate with Medical Affairs, Clinical Development, Clinical Operations, and Commercial teams.

• Establish and maintain strategic relationships with Key Opinion Leaders (KOLs) and institutional stakeholders.

• Oversee site readiness and the integration of workflows for both approved agents and clinical trials, focusing on product handling, administration, radiation safety, and licensing issues.

• Provide clinical and technical education to ensure safe, effective, and guideline-compliant product use.

• Keep up-to-date as a subject-matter expert in nuclear medicine, radiopharmaceutical applications, imaging methodologies, oncology practice patterns, and emerging therapeutic developments.

• Assist in the execution of clinical trials through site training and protocol education.

• Address unsolicited scientific inquiries with precise documentation and adherence to regulatory standards.

• Collect field insights on diagnostic imaging and radiopharmaceutical trends, institutional challenges, and adoption patterns.

• Offer support for medical and scientific congresses as needed.

• Ensure compliance with Standard Operating Procedures (SOPs) and relevant regulatory frameworks.

• Utilize AI to enhance team performance and decision-making processes.


⛳️ Requirements

• A bachelor's degree is required.

• CNMT certification is preferred.

• A minimum of 7 years of experience in nuclear medicine, radiopharmaceutical clinical applications, oncology imaging, or a related discipline.

• Proven experience in leading complex site education and workflow implementation projects.

• Advanced comprehension of radiopharmaceutical science, nuclear medicine operations, and diagnostic imaging trends.

• Capability to convert intricate data into actionable, site-specific execution strategies.

• Strong executive presence with the ability to forge institutional relationships.

• Experience in a cross-functional role within a matrixed biotech or pharmaceutical setting.

• Exceptional communication, presentation, and organizational abilities.

• Background in oncology and radiopharmaceuticals is highly preferred.

• Must adhere to the U.S. Compliance Code of Conduct, OIG Guidance, PhRMA Code, GCP, HIPAA, and applicable FDA regulations.


🏝️ Benefits

• Additional discretionary cash and stock incentives.

• Support for wellbeing.

• Retirement and financial protection benefits.

• Comprehensive medical, dental, vision, life, and disability insurance options.

• Flexible Time Off (FTO) policy without an 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 available for eligible employees.

• Paid sick leave.

• Up to two paid volunteer days per year.

• Flexible summer hours.

• Leaves of absence for medical, personal, parental, caregiver, bereavement, and military reasons.

• Annual Global Shutdown occurring between Christmas Day and New Year's Day.

• Reasonable workplace accommodations and ongoing support for individuals with disabilities.

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