Associate Director, Radiopharmaceutical Clinical Applications – Northeast

Remote Full-time
Job Description:
• Identify, develop, and engage in long-term relationships with Key Opinion Leaders (KOLs) and Healthcare Providers (HCPs) in the assigned territory, including Nuclear Medicine Physicians, Radiologists, Radiation Oncologists, Technologists, Safety Officers, Health Physicists, Nursing Staff, and Advanced Practice HCPs at imaging facilities and medical centers.
• Provide training to imaging/treatment centers on handling, administration, and radiation safety of current products, including initial and re-training sessions.
• Educate on-site preparation and infusion processes for products, including radiopharmaceutical licensing, supporting approved imaging/therapies, and clinical trials.
• Educate the HCP community to ensure they have the proper knowledge and technical expertise to use Lantheus products safely and effectively.
• Utilize clinical and technical expertise to institutional workflows, regional diagnostic imaging patterns, treatment guidelines, and therapeutic advances in oncology and molecular imaging.
• Gather insights into the needs and interests of healthcare providers and the medical needs of patients with a focus on Lantheus approved and investigational agents.
• Maintain thorough and up-to-date knowledge of imaging techniques, clinical information, and product data in the diagnostic and therapeutic radiopharmaceutical field.
• Respond appropriately and document accurate scientific data in response to unsolicited questions from customers about approved and investigational products.
• Support Lantheus Field Research Initiatives, including Investigator Sponsored Trials (ISTs), the Image Library, and Clinical Trials aligned with the Lantheus pipeline.
• Attend national congresses and meetings, providing medical and scientific booth support as requested, in compliance with industry regulations.
• Fully understand and comply with all Lantheus SOPs, working procedures, and corporate requirements.
• Adhere to the US “Compliance Code of Conduct” and all LMI policies and procedures, the OIG Guidance, the PhRMA Code, GCP, HIPPA and relevant FDA laws and regulations (certify completion where required).

Requirements:
• Minimum Bachelor’s Degree Required
• 4+ years Nuclear Medicine Technologist, Clinical Application Specialist, or similar/relevant experience.
• 2+ years Clinical experience in oncology, urology, neurology or radiopharmaceuticals/medical imaging
• Exceptional communicator and presenter with proven oral and written communications skills.
• Advanced understanding of current and emerging trends in the field of Nuclear Medicine, radiopharmaceuticals, and diagnostic imaging.
• Proficient at translating and communicating approved scientific or clinical data into high quality medical information appropriate to the audiences engaged.
• Demonstrated success working in a team environment, communicating clearly and effectively with management, peers, and all cross-functional teams.
• Highly motivated to achieve optimal results with a demonstrated record of career growth and achievement.
• Proven ability to successfully manage multiple tasks simultaneously and adapt to and communicate change.
• Advanced Word, PowerPoint, and Excel skills
• 60% Travel required; reside near an international airport

Benefits:
• comprehensive health benefits package that includes medical, prescription drug, dental, and vision coverage
• life and disability benefits
• pre-tax accounts
• 401(k) with company contribution
• a variety of other benefits
• generous time off package including paid vacation, holidays, sick days, and paid parental leave

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