Clinical Consultant - Genetic Testing Clinical Report Sign out
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How You’ll Contribute
- Case Review & Signout:
- Review and approve variant classifications and genetic reports for germline hereditary testing.
- Ensure reporting is accurate, evidence-based, and presented with appropriate clinical nuance for maximal utility to patients and providers.
- Collaborate with variant scientists and genetic counselors on complex and challenging cases.
- Leadership & Cross-Functional Collaboration:
- Participate in continuous improvement of policies and best practices in clinical reporting.
- Provide clinical oversight for validation of new assays and updates to existing workflows.
- Maintain a basic understanding of bioinformatics pipelines to inform interpretation and reporting, ensuring concordance between analytic pipelines and clinical sign-out.
- Collaborate with laboratory operations, laboratory director, QA, and bioinformatics teams to ensure consistency and accuracy in data analysis and reporting.
What We’re Looking For:
- Education & Certification
- M.D. Molecular Pathologist with genetic testing experience and an active license to practice in the State of California, Ph.D.
- Medical Geneticist with ABMGG (or equivalent) certification in Clinical Molecular Genetics / Laboratory Genetics & Genomics and California CGMB license
- Experience
- Experience in a clinical molecular genetics laboratory, with responsibility for case sign-out, variant interpretation, and regulatory compliance.
- Extensive expertise with germline hereditary cancer testing, NGS-based workflows, and laboratory quality systems.
- Familiarity with supporting technologies (Sanger sequencing, MLPA, arrayCGH, long-read sequencing) is a plus.
- Experience in high-throughput environments is preferred.