Laboratory Director

Responsibilities

• Provide clinical sign-out and interpretation for CGP reports, identifying actionable biomarkers and relevant clinical trials
• Provide technical and clinical support for laboratory staff, genetic counselors, and other clinical personnel
• Ensure acceptable levels of analytical performance for CGP assays and compliance with applicable standards
• Troubleshoot workflow and laboratory issues with clinical care and regulatory standards in mind
• Document findings and maintain accurate records consistent with company policies
• Serve as a Clinical Consultant to ensure test reports include pertinent information for interpretation

Requirements

• MD/DO and/or PhD in genetics or related field
• ABMGG board certification in Clinical Cytogenetics and/or Molecular Genetics, or ABP board-certified in Molecular Genetic Pathology
• Current California laboratory director license (or eligibility)
• Current NYS CLEP Certificate of Qualification in Genetic Testing (or eligibility)
• Minimum 5 years of experience in a CLIA-certified clinical laboratory setting
• Deep knowledge of CAP, CLIA, California, and New York state regulations
• Demonstrated management experience in a high-throughput clinical laboratory

Preferred Qualifications

• Understanding of Illumina sequencing platforms, liquid biopsy (ctDNA), and tissue-based CGP assays
• Familiarity with professional guidelines for somatic variant interpretation (e.g., AMP/ASCO/CAP tiering)
• Understanding of statistical measures and bioinformatic concepts used in genetic testing

About the Company

Natera is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health, aiming to make personalized genetic testing a standard of care.