Research Nuclear Medicine Coordinator

BAMF Health • Grand Rapids, MI

1d • Onsite

About The Position

Join BAMF Health, where you're not just part of a team; you're at the forefront of a revolution in Theranostics, changing lives for the better. As a member of our global team, you'll contribute to pioneering technology and deliver top-tier patient care. Located in the heart of downtown Grand Rapids, our cutting-edge global headquarters resides within the state-of-the-art Doug Meijer Medical Innovation Building. Step into our modern and spacious facilities, where innovation thrives and collaboration knows no bounds. Join us in our mission to make Theranostics accessible and affordable for all, and be part of something truly remarkable at BAMF Health. The Nuclear Medicine Research Coordinator is responsible for supporting research for molecular Imaging and radioligand therapy clinical trials from start up through completion. May assist or perform study procedures—molecular imaging, administration of imaging or therapy agents, or PK dosimetry of research radiopharmaceuticals. Responsible for nuclear medicine and molecular imaging activities for start-up of new trials. Using technical expertise, determine project feasibility and identify resource needs and costs, and develop and execute a start-up plan. Collaborate with researchers and clinicians to support the development and implementation of innovative nuclear medicine imaging protocols and techniques for clinical studies and research projects. In coordination with the Research RNs/Coordinators and Start Up Teams, correspond with sponsors and vendors to facilitate trial start up and execution. Responsible for collaborating with sponsors, Contract Research Organizations (CROs), and camera vendors to develop camera protocols. Responsible for developing and implementing camera protocols, writing clinical guidelines and checklists for clinical trial rollout, and leading nuclear medicine staff education. Responsible for oversight or conducting all camera and hotlab equipment qualification testing. Responsible for receipt and handling of radiopharmaceutical investigative products (IP). Provide training and ongoing support to nuclear medicine staff on the operation, interpretation, and clinical applications of nuclear medicine equipment and software. Answering/correcting any data/imaging queries from the Sponsor/CRO; uploading data to external web portals for Sponsor/CRO. Provide clear and concise communication, including complex technical details to internal and external stakeholders with limited knowledge of nuclear medicine or molecular imaging and theranostics.

Requirements

• Associate of Science Degree in Nuclear Medicine required
• 5 years of related experience required
• Certified Nuclear Medicine Technologist by the American Registry of Radiologic Technologist (ARRT) OR Certified Nuclear Medicine Technologist by the Nuclear Medicine Technology Certification Board (NMTCB) required
• Basic Life Support (BLS) within 30 days of hire required

Nice To Haves

• Bachelor of Science Degree Nuclear Medicine preferred
• 10 years of related experience preferred
• SOCRA Certified Clinical Research Professional (CCRP) or ACRP Certified Professional (ACRP-CP) or ACRP Certified Clinical Research Coordinator (CCRC) preferred

Responsibilities

• Supporting research for molecular Imaging and radioligand therapy clinical trials from start up through completion.
• Assist or perform study procedures—molecular imaging, administration of imaging or therapy agents, or PK dosimetry of research radiopharmaceuticals.
• Responsible for nuclear medicine and molecular imaging activities for start-up of new trials.
• Using technical expertise, determine project feasibility and identify resource needs and costs, and develop and execute a start-up plan.
• Collaborate with researchers and clinicians to support the development and implementation of innovative nuclear medicine imaging protocols and techniques for clinical studies and research projects.
• In coordination with the Research RNs/Coordinators and Start Up Teams, correspond with sponsors and vendors to facilitate trial start up and execution.
• Responsible for collaborating with sponsors, Contract Research Organizations (CROs), and camera vendors to develop camera protocols.
• Responsible for developing and implementing camera protocols, writing clinical guidelines and checklists for clinical trial rollout, and leading nuclear medicine staff education.
• Responsible for oversight or conducting all camera and hotlab equipment qualification testing.
• Responsible for receipt and handling of radiopharmaceutical investigative products (IP).
• Provide training and ongoing support to nuclear medicine staff on the operation, interpretation, and clinical applications of nuclear medicine equipment and software.
• Answering/correcting any data/imaging queries from the Sponsor/CRO; uploading data to external web portals for Sponsor/CRO.
• Provide clear and concise communication, including complex technical details to internal and external stakeholders with limited knowledge of nuclear medicine or molecular imaging and theranostics.

Benefits

• Employer paid High Deductible Health Plan with employer HSA contribution
• Flexible Vacation Time
• 401(k) Retirement Plan with generous employer match
• Several benefit options including, but not limited to; dental, vision, disability, life, supplemental coverages, legal and identity protection
• Free Grand Rapids downtown parking

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree