Job Description:
• 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.
• 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.
Requirements:
• 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 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.
Benefits:
• bonus
• equity
• benefits
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