Advanced Medical Imaging Professional

6 days ago

Thāne, Maharashtra, India beBeeNuclear Full time ₹ 90,00,000 - ₹ 1,20,00,000
Nuclear Medicine Imaging Specialist

This role involves conducting quality control and analysis procedures, as well as providing medical writing support at a clinical trial level.

Key Responsibilities:
  • Perform technical quality review of images per trial specifications
  • Perform Quantitative image analysis
  • Manage research projects and early phase clinical trials for day-to-day activities
  • Complete quality control documentation according to standard operating procedures
  • Develop quality control documentation in conjunction with the Project Manager
  • Generate image queries to address technical issues, track those issues and ensure timely resolution
  • Clinical site and imaging center support
  • Creation and review of imaging site questionnaires
  • Develop training materials for imaging site personnel including Data Transmittal Form, Imaging Manual, Site Training slides, and other supplemental documents as needed
  • Technical training of imaging site personnel (on-site or telecon)
  • Collaborate with project internal teams to support sponsor specified project scope of work as required
  • Provide medical and scientific input to the following documents as necessary/applicable
  • Project Management Plans
  • Imaging Review Charters
  • Reader Rules
  • Image Analysis Platform
  • Final Study Reports
  • Clinical Case Report Forms
  • Study Protocols
    • Monitor/evaluate reader results to ensure compliance with protocol criteria and CRF completion requirements
    • Mentor and assist in the training of internal staff
    • Other duties as assigned by manager
    Requirements:
    • Registered Nuclear Medicine Technologist
    • Knowledge of PET/CT imaging systems required
    • Knowledge of SPECT imaging systems preferred
    • Associates or Bachelor's degree preferred
    • Minimum of 3 years' experience as a nuclear medicine technologist required
    • Minimum of 1 year of experience in the clinical trials industry preferred
    • Knowledge of Good Clinical Practice (GCP), Quality Assurance/Compliance in a clinical trials setting is preferred
    • Knowledge of image trial documents strongly preferred, i.e., Image Review Charter, Imaging Manual, Data Transmittal Forms, etc.
    • Prior Project Management duties preferred, i.e., driving timelines, deliverables and managing concurrent priorities

    This role requires strong analytical and problem-solving skills, as well as excellent communication and interpersonal skills. If you are a motivated and detail-oriented individual who is passionate about advancing clinical trials and improving patient outcomes, we encourage you to apply for this exciting opportunity.

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