Laboratory Director

Minimum of 5 years of experience in a CLIA-certified clinical laboratory setting analyzing, interpreting and reporting clinical genetic/genomic data.

Demonstrated management experience in a high-throughput clinical laboratory environment.

Solid understanding of Illumina sequencing platforms, liquid biopsy (ctDNA), and tissue-based CGP assays.

Strong familiarity with professional guidelines for somatic variant interpretation (e.g., AMP/ASCO/CAP tiering).

Understanding of statistical measures and bioinformatic concepts utilized in genetic testing, variant calling, and screening.

This range reflects a good-faith estimate of the base pay we reasonably expect to offer at the time of  hire. Final compensation will vary based on experience, qualifications, and internal equity considerations.

This position is also eligible for additional compensation and benefits through Natera’s robust Total Rewards program, including:

Annual performance incentive bonus

Long-term equity awards

401(k) with company match

As an Associate Lab Director or Lab Director of Oncology, you have clinical oversight of Natera’s laboratory testing related to cancer testing.  You ensure that testing is properly performed, and applicable regulatory standards are met.  You are responsible for ensuring that the laboratory implements testing while consistently providing accurate and reliable patient test results.  You are responsible for ensuring the test validation and development meets all required regulatory standards.  This position will be primarily responsible for technical and clinical performance of Natera’s comprehensive genomic profiling (CGP) assays.  Title and scope of responsibility will be commensurate with the candidate’s experience.  This position is on-site at Natera’s San Carlos, CA Laboratory.

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, compliance with applicable standards, and laboratory inspection-readiness at all times

Troubleshoot workflow and laboratory issues with clinical care and regulatory standards in mind

Document findings and maintain accurate records consistent with Natera policies and procedures