Director - Cytogenetics

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    "description": "<p><strong>About Us</strong></p>\n\n<p><strong>CSI Laboratories, a Fulgent Genetics Company, </strong>is a nationally recognized cancer testing and diagnostics laboratory experienced in helping pathologists and oncologists diagnose and treat cancer patients.</p>\n\n<p>Founded in 2011, our parent entity, Fulgent Genetics, has evolved into a premier full-service genomic testing company built around a foundational technology platform.&nbsp;</p>\n\n<p>Through our diverse testing menu, Fulgent is focused on transforming patient care in oncology, anatomic pathology, infectious and rare diseases, and reproductive health. We believe that by providing a wide range of effective, flexible testing options in conjunction with best-in-class service and support, we can redefine the way medicine is managed for patients and clinicians alike.</p>\n\n<p>Since integrating with our therapeutic development business, Fulgent is also developing drug candidates for treating a broad range of cancers using a novel nanoencapsulation and targeted therapy platform. By merging our fields of expertise, we aim to become a fully integrated precision medicine company.</p>\n\n<p>&nbsp;</p>\n\n<p><strong>Summary of Position</strong></p>\n\n<p>Responsible for review and sign out of cytogenetic and fluorescent in-situ hybridization (FISH) cases.</p>\n\n<p>&nbsp;</p>\n\n<p><strong>Key Job Elements</strong></p>\n\n<ul>\n\t<li>Responsible for review and sign out of cytogenetic and FISH cases.</li>\n\t<li>Application of accepted criteria in formulating and reporting diagnostic/prognostic information on various specimens including hematologic and solid tumor specimens.</li>\n\t<li>Ensure that the reports of test results include pertinent information required for interpretation.</li>\n\t<li>Collaboration with hematopathologists and surgical pathologists to provide appropriate diagnostic and prognostic interpretation.</li>\n\t<li>Interpretation/sign-out of pathology specimens within CAP guidelines for turnaround time.</li>\n\t<li>Provide clinical laboratory consultation to technical personnel and healthcare providers.</li>\n\t<li>Participation in Quality Assurance measures for the laboratory as required by accreditation standards.&nbsp;</li>\n\t<li>Provide residents and/or trainees information on specimen evaluation and reporting as needed.</li>\n\t<li>Provide on-call services as designated in department schedule.</li>\n\t<li>Support with guidance and training of the Genetics analysis technologists, as needed.</li>\n\t<li>Perform other responsibilities as requested or required by CLIA and other local, state, or federal regulations.</li>\n</ul>\n",
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