About this role
Role Overview
Apply hands-on Visage 7 expertise to evaluate imaging records, study interpretation workflows, and documentation quality. This remote, hourly role focuses on ensuring imaging findings, comparisons, measurements, and follow-up actions are accurate, persistent, traceable, and ready for downstream clinical use.
Key Responsibilities
- Establish a patient''s imaging status as of the relevant study date and compare it with the appropriate prior study, rather than simply the latest prior.
- Evaluate multi-series and multi-timepoint studies, including when additional imaging, critical-results communication, subspecialty review, or routine sign-off is appropriate.
- Assess quantitative imaging work when applicable, including RECIST/PERCIST tracking, SUV values and calibration dependencies, vessel and volume measurements, and fusion or registration accuracy.
- Confirm that patient, study, series, and instance records and identifiers, including MRN, accession number, Study Instance UID, and procedure code, are accurate and connected.
- Record interpretation and communication history accurately, including partial, preliminary, and handed-off information, and set or interpret follow-up recommendations, flags, and recall dates.
- Review worklist construction, filters, study-status transitions, study claiming and release practices, and the commitments associated with wet reads, preliminary reads, and final reports.
- Determine what is confirmed versus assumed when taking over a mid-read study or shift handoff, and investigate missing expected priors using relevance and fetching rules.
- Apply hanging protocols, display protocols, window and level presets, procedure and protocol mappings, series descriptions, and DICOM tag knowledge to identify mis-hung, mis-labeled, or mis-routed studies.
- Consider related RIS/EHR orders, dictation systems, and AI-result overlays where relevant.
- Apply organizational protocol, dose, and reporting standards to assess whether a study is complete and interpretable, using the protocol, template, or criteria set in effect on the study date.
- Apply relevant MQSA, ACR accreditation and dose registry requirements, critical-findings communication policies, and information-blocking and patient-release rules.
- Document findings, measurements, key images, and unresolved items so subsequent readers, ordering clinicians, and tumor boards can understand conclusions and outstanding work.
- Verify the persistence of annotations, presentation states, and key-image selections, and support peer-review, discrepancy, amendment, audit-trail, and access-logging workflows.
- Confirm that the imaging record reflects what was acquired and concluded, distinguish session-only actions from record-persistent actions, assess study completeness, and ensure recorded outcomes are reproducible and auditable.
Qualifications
- Regular Visage 7 use, at least weekly, in a current or recent professional role.
- At least 2 years of professional experience in diagnostic radiology, imaging technology, imaging operations, PACS, or imaging informatics.
- Strong working familiarity with study-status transitions, prior-study comparison, and the distinction between preliminary and final results.
- MD or DO with radiology residency or fellowship training, with board certification or eligibility preferred, or an ARRT, RDMS, NMTCB, or equivalent technologist credential with hands-on advanced-visualization experience, or a bachelor''s degree in health informatics, medical imaging, computer science, or a related field plus CIIP, PARCA, or equivalent hands-on PACS administration experience.
Work Terms
- Remote hourly engagement.
- Ongoing familiarity with Visage 7 is required through weekly or more frequent use.
Compensation
$90 to $130 per hour.
Eligibility
Eligibility is based on meeting the required current or recent Visage 7 usage and relevant professional imaging experience.