{"html":"<h4>Core (required of all candidates)</h4>\n<ul>\n<li><p>Knows how to work accessioning end to end: order entry, specimen labeling, requisition and insurance capture, and specimen rejection criteria</p>\n</li>\n<li><p>Knows how to review results before release (QC status, delta checks, critical values, instrument flags) and when a result must be held</p>\n</li>\n<li><p>Knows how reflex and confirmation testing work (for example, screen-positive to confirmation in toxicology) and when one should have been triggered</p>\n</li>\n<li><p>Knows how to trace a specimen and its chain of custody through the lab, and catch mislabeled or mismatched specimens</p>\n</li>\n<li><p>Knows how corrected and amended reports work, and who must be notified when a released result changes</p>\n</li>\n</ul>\n<h4>Specialized depth (strong working knowledge in at least 2–3 of the following)</h4>\n<ul>\n<li><p>Toxicology (immunoassay screening, LC-MS/MS confirmation, cutoffs)</p>\n</li>\n<li><p>Molecular, PCR, and infectious disease testing</p>\n</li>\n<li><p>Pharmacogenomics (PGx)</p>\n</li>\n<li><p>Clinical chemistry and hematology</p>\n</li>\n<li><p>Instrument interfacing and LIS configuration (test codes, panels, reference ranges)</p>\n</li>\n<li><p>Billing and medical necessity (CPT, ICD-10, ABN)</p>\n</li>\n<li><p>CLIA and CAP compliance and inspection readiness</p>\n</li>\n</ul>\n<p>What you&#39;ll do</p>\n<ul>\n<li><p>Confirm that an accession, result, or report in the LIS is correct and releasable, not just entered</p>\n</li>\n<li><p>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</p>\n</li>\n<li><p>Judge completeness: are all tests on the order, all specimens, and all required notifications handled</p>\n</li>\n<li><p>Distinguish &quot;the LIS accepted it&quot; from &quot;a lab director would sign off on it&quot;</p>\n</li>\n<li><p>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</p>\n</li>\n</ul>\n<p>Requirements</p>\n<ul>\n<li><p><strong>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</strong></p>\n</li>\n<li><h4>2+ years of experience in a CLIA-certified clinical laboratory</h4>\n</li>\n<li><p>Can spot a QC failure, a missed reflex, or a mislabeled specimen on sight</p>\n</li>\n<li><p>MLS/MT (ASCP) certification or equivalent state licensure; lab supervisor, LIS analyst, or lab director experience is a plus</p>\n</li>\n<li><p>Strong working knowledge in at least 2–3 specialized areas above</p>\n</li>\n<li><p>Prior data annotation, labeling, or AI evaluation experience is a plus</p>\n</li>\n</ul>"}