Clinical Consultant – Genetic Testing

Job not on LinkedIn

October 27

🏄 California – Remote

Although this job is listed in California, this company may be open to hiring remote in other states.

⏱ Part Time

🟡 Mid-level

🟠 Senior

💼 Consultant

🦅 H1B Visa Sponsor

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Color

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Color Health provides the infrastructure to support durable and equitable public health across entire populations. Color’s technology and clinical services are the backbone of large-scale population health programs for over 200 institutions worldwide, with data and services spanning hereditary cancers, heart disease, infectious disease testing (including COVID-19), and community-based vaccination programs. Using a data driven approach, we’re democratizing access to health care insights.

501 - 1000 employees

📋 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