Pay: $70 – $100/hour
Commitment: Hourly, ~40 h/week
Field: Medicine
To qualify you must use Dendi LIS or another laboratory information system regularly - weekly or more - as a working part of your job, with 2+ years of experience in a CLIA-certified clinical laboratory.
Core (required of all candidates)
- Knows how to work accessioning end to end: order entry, specimen labeling, requisition and insurance capture, and specimen rejection criteria
- Knows how to review results before release (QC status, delta checks, critical values, instrument flags) and when a result must be held
- Knows how reflex and confirmation testing work (for example, screen-positive to confirmation in toxicology) and when one should have been triggered
- Knows how to trace a specimen and its chain of custody through the lab, and catch mislabeled or mismatched specimens
- Knows how corrected and amended reports work, and who must be notified when a released result changes
Specialized depth (strong working knowledge in at least 2–3 of the following)
- Toxicology (immunoassay screening, LC-MS/MS confirmation, cutoffs)
- Molecular, PCR, and infectious disease testing
- Pharmacogenomics (PGx)
- Clinical chemistry and hematology
- Instrument interfacing and LIS configuration (test codes, panels, reference ranges)
- Billing and medical necessity (CPT, ICD-10, ABN)
- CLIA and CAP compliance and inspection readiness
What you'll do
- Confirm that an accession, result, or report in the LIS is correct and releasable, not just entered
- Catch results released despite a QC failure, missed reflex or confirmation tests, mismatched specimens, and changes to records the task did not ask to touch
- Judge completeness: are all tests on the order, all specimens, and all required notifications handled
- Distinguish "the LIS accepted it" from "a lab director would sign off on it"
- Verify that a request that should be refused (releasing a result with failed QC, editing a released result without a corrected report) is refused rather than forced through
Requirements
- Frequent use of Dendi LIS or another LIS (e.g., Orchard Harvest, Epic Beaker, Sunquest, Cerner PathNet, LabWare, XiFin) - weekly or more - in your current or recent role
- 2+ years of experience in a CLIA-certified clinical laboratory
- Can spot a QC failure, a missed reflex, or a mislabeled specimen on sight
- MLS/MT (ASCP) certification or equivalent state licensure; lab supervisor, LIS analyst, or lab director experience is a plus
- Strong working knowledge in at least 2–3 specialized areas above
- Prior data annotation, labeling, or AI evaluation experience is a plus
Vacancy posted 3 days ago
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