Oncology Imaging Quality Control Specialist II (US Remote)

MERIT CRO, Inc.Madison, WI
Remote

About The Position

MERIT CRO, Inc. is seeking a full-time Oncology Imaging Quality Control Specialist II to perform duties of the Imaging Quality Control Specialist (IQCS) I role, create and conduct training for internal departments, and potentially conduct clinical site certification activities. The primary functions include processing clinical trial data in the EXCELSIOR™ cloud application environment, performing data upload, error resolution, clinical data analysis, and data quality evaluation according to MERIT and/or study-specific procedures and Good Clinical Practices (GCP). This role emphasizes collaboration, customer focus, and creative problem-solving.

Requirements

  • Minimum of five (5) years of work experience in a hospital, research hospital, or freestanding radiology facility.
  • A bachelor's degree is required.
  • Experience as a technologist in an imaging center or Contract Research Organization (CRO) is required.
  • Strong interpersonal and organizational skills.
  • Excellent attention to detail.
  • Ability to follow directions.
  • Ability to assess Company needs and work independently.
  • Computer skills including proficiency in Microsoft Office software.
  • Ability to learn Company specific software.
  • Must be able to project a professional attitude and image appropriate for the work environment.
  • Ability to participate and contribute in a team environment as a team member.
  • Oral and written communication is clear, concise, and effective.
  • Current certification in at least one modality (PET and/or Nuclear Medicine) from an organization such as the Nuclear Medicine Technology Certification Board (NMTCB), or the American Registry of Radiologic Technologists (ARRT), or other applicable nationally recognized certifying agency.
  • Regularly use hands to touch, finger, grasp, handle or feel, with repetitive motions, and talk or hear.
  • Ability to utilize a computer to carry out all assigned or described job duties; type, view screen, adjust peripherals, etc.
  • Ability to stand and walk and sit.
  • Specific vision abilities required include close vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.

Nice To Haves

  • Experience in clinical trial imaging is highly preferred.
  • Experience with SPECT imaging and dosimetry is a plus.
  • A minimum of one (1) year of clinical, clinical trial, or data quality experience in a related field along with education may be considered.

Responsibilities

  • Monitor own work to ensure quality and completeness.
  • Prioritize tasks by order of importance and deadlines.
  • Identify and correct errors swiftly.
  • Work with limited supervision.
  • Perform initial clinical data check-in (review) and quality control per training and project-specific requirements.
  • Issue and review data queries to ensure completeness and accuracy of response relative to other data.
  • Assist in development of project and regulatory documents, including proofreading.
  • Assist with the development/implementation of training programs.
  • May serve as a Subject Matter Expert to conduct training for check-in and quality control.
  • Understand the EXCELSIOR™ product, protocol, and conduct of clinical trials to discuss tasks with team members and sponsors.
  • Organize and prioritize work assignments to complete tasks on time with quality, and anticipate problem areas.
  • Apply creative approaches and ideas to solve problems, maximizing effective use of resources.
  • Independently process clinical data from start-up through study close out, prioritizing work to meet project timelines.
  • Follow regulatory guidelines regarding Protected Health Information (PHI).
  • May conduct clinical site technician and equipment certification.
  • Provide customer service for the EXCELSIOR™ software application related to responsibilities.
  • Provide additional support to contracted readers as applicable.
  • Review, categorize, and respond to customer support and complaint tickets in the helpdesk application.
  • May be asked to author procedure manuals for external distribution.
  • Comply fully with company policies and Standard Operating Procedures (SOPs).
  • Practice and respond with commitment and sensitivity toward satisfying the needs of internal and external customers.
  • Promote quality and continuous improvement philosophy.
  • Complete work in a timely manner.
  • Interact with clients and co-workers in a professional manner.
  • Demonstrate a commitment to maintain a safe, clean, and orderly work area.
  • Promote and follow safety regulations and actively contribute to work safety.

Benefits

  • 401(k) Retirement Plan
  • Dental insurance
  • Health insurance
  • Paid Life insurance & AD&D
  • Paid Long-Term Disability
  • Paid Time Off (Vacation and Sick)
  • Paid 8 Holidays
  • Vision insurance
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