Responsibilities- Assist in the development of, and adherence to, imaging trial documents (e.g., Image Review Charter, Imaging Manual, Data Transmittal Forms, and Dosimetry Manuals).
- Provide subject matter expertise to internal and external stakeholders in matters of image acquisition, storage, review, and processing.
- Maintain an archive of imaging related data for ongoing and completed trials.
- Collaborate with clinical operations in the oversight, conduct and management of imaging-related aspects of clinical studies in accordance with the clinical protocol, study manuals and plans, and timelines while ensuring quality in accordance with GCP and ICH guidelines.
- Assist with the management of in-house processing of image data and internal dosimetry efforts to support ongoing research and multi-disciplinary department and company initiatives.
- Provide support for clinical data review; assist in generation of clinical research reports and presentations including abstracts, posters, and publications.
- Provide support to clinical site staff and investigators pertaining to preparation, administration, and waste management of imaging and therapeutic radiopharmaceuticals.
- Respond to radiation safety questions and concerns regarding the use of diagnostic and therapeutic radiopharmaceuticals and precautions.
- Have a working knowledge and understanding of modern electronic infrastructures relevant to radiological imaging such as DICOM, PACS, IHE models, image processing and advanced visualization.
- Willingness to travel when needed (5-10%)
Qualifications - The candidate should have a Bachelor of Science degree with a life science focus from an accredited educational institution and NMTCB/ARRT(N) certification in nuclear medicine or equivalent. Additional training in radiation safety (NMTCB(RS)) and/or medical physics with an advanced master's qualifications is preferred but not required.
- Minimum of at least 5 years of clinical experience.
- Experience working in clinical trials for 2-5 years is preferred but not required.
- Demonstrated technical and analytical problem-solving skills.
- Scientific expertise in SPECT and PET imaging is recommended, including acquisition, reconstruction and uploading of images.
- Training in Good Clinical Practices (GCP), Quality Assurance/Compliance (QA/QC) in a clinical trial setting is preferred.
- Experience with radioactive materials license amendment process with the NRC and Agreement States.
- Familiar with Radiation Safety Officer (RSO) responsibilities.
- Ability to clearly articulate and present the role and impact of molecular imaging on decision making within drug discovery and development.
- Self-motivation and exceptional verbal and written communication skills.
- Ability to multi-task and work effectively in a team or independently on assigned tasks.
- Proficiency in business computer skills and experience with medical imaging workstations
- (i.e., MIM), dosimetry software, and/or PACS preferred.
The annual base pay for this position ranges from $118,870.40 to $178,305.60. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted19-Aug-2026
Closing Date11-Sep-2026
