
Nuclear Medicine Technologist – Theranostics
Posted 4 days ago

Posted 4 days ago
This is a fully remote position, open to applicants in California.
• Lead and manage the strategic onboarding process for new imaging sites, ensuring the smooth integration of Telix radiopharmaceuticals into both commercial and clinical trial workflows.
• Create and implement best practices for optimizing imaging sites, including standardization of protocols, scanner settings, and enhancements in workflow efficiency to achieve superior imaging outcomes.
• Supervise and execute essential field activities in accordance with the Medical Affairs strategy, providing optimal support for product launches, clinical research, and physician education.
• Actively influence the development of research priorities by identifying significant data gaps, opportunities for real-world evidence, and medical insights, ensuring alignment with Telix’s scientific and commercial goals.
• Spearhead site engagement strategies, collaborating closely with imaging centers, nuclear medicine specialists, and key stakeholders to guarantee optimal patient access and product utilization.
• Establish and maintain a structured framework for scientific education, creating training materials, presenting medical and product information, and ensuring consistent knowledge transfer to both internal and external stakeholders.
• Represent Telix Medical Affairs at prestigious medical/scientific meetings, gathering and synthesizing insights that inform company strategy and future product development.
• Remain up-to-date on imaging best practices and emerging technologies.
• Serve as a vital liaison between Medical Affairs and cross-functional teams, ensuring alignment with Commercial, Marketing, Clinical Operations, and Regulatory teams.
• Oversee key projects and initiatives within the Medical Affairs function, ensuring efficient execution and measurable contributions to Telix’s strategic objectives.
• Ensure compliance with pharmaceutical regulations, corporate policies, and ethical guidelines, proactively addressing any training or adherence gaps.
• BS or MS degree in a scientific field (preferably Radiology or similar) or equivalent experience is required.
• Certification from the Nuclear Medicine Technology Certification Board (NMTCB) or the American Registry of Radiologic Technologists (ARRT) is mandatory.
• A minimum of 5 years of experience in advanced oncology PET scanning and optimization is required.
• Experience in radiopharmaceuticals is essential, with a preference for prostate cancer expertise.
• Comprehensive understanding of relevant policies governing the Pharmaceutical Industry.
• Expertise in interpreting scientific data, conducting market research, and utilizing competitive intelligence tools.
• Proficient in Microsoft Office Suite.
• Proven ability to deliver results that meet or exceed targeted objectives.
• Exceptional verbal and written communication skills.
• Strong skills in multi-tasking, time management, organization, interpersonal relations, business acumen, and a high level of emotional intelligence.
• Detailed knowledge of regulations and best practices regarding industry interactions with healthcare professionals.
• Capacity to take initiative and work both independently and collaboratively in a team setting.
• Ability to quickly grasp complex disease areas, treatments, clinical development plans, healthcare landscapes, hospitals, healthcare professionals, and the patient journey.
• A valid driver's license is required.
• Willingness to travel locally, regionally, and nationally up to 75%.
• Must reside in close proximity to a major airport.
• Competitive salaries.
• Annual performance-based bonuses.
• Equity-based incentive program.
• Generous vacation policy.
• Paid wellness days.
• Support for learning and development.
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