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Anatomic Pathologist

Successful applicants for this position must be fully vaccinated against COVID-19 as a condition of employment. Vaccine verification will be required. 


As the Pathologist and one of our pathologists, you have clinical oversight of Natera’s laboratory 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 will also be responsible for the proper maintenance of the histology lab for FFPE tissue block processing, slide staining/coverslipping/scanning, and performance evaluation of the HistoTechs (HTs and/or HTLs) and other lab personnel. 

  • Review patient specimens prior to testing in collaboration with other applicable stakeholders.
  • Review clinical notes (e.g., chief complaint and treatment history) and pathology reports for tumor information (primary location, histologic type and sample location [primary vs metastatic]) and perform tumor circling on H&E slides for molecular testing; and help to identify an alternative optimal FFPE block(s) and/or tumor specimen if the current sample is inadequate.
  • Review, approve, and sign-out reports for oncology testing, mainly on NGS platforms, but may also include SNP array analysis and other methodologies.
  • Oversee the review of genetic and CNV variant data: interpret NGS and microarray results in the context of medical literature, online variant databases and other references along with relevant patient demographic data.
  • Provide clinical and technical support for genetic counselors and other laboratory personnel. Set standards for laboratory testing and acceptable levels of analytic performance and ensure these are maintained. 
  • Analyze lab data, contribute to or write publications for high-quality scientific journals.
  • May serve as Clinical Consultant. The Clinical Consultant is responsible for ensuring:
  • the proper utility of our assays including sample selection, and test appropriateness,
  • test reports include pertinent information for test interpretation, and
  • availability for consultation concerning test results and the interpretation of those results as they relate to specific patient conditions.
  • May serve as Technical Supervisor. The Technical Supervisor is responsible for ensuring:
  • appropriate test method selection;
  • adequate method verification to determine the accuracy and precision of the test;
  • enrollment of the laboratory in a CMS-approved proficiency testing (PT) program for the test performed;
  • PT samples are tested in accordance with the CLIA requirements;
  • PT results are returned within the time frames established by the PT program;
  • PT reports are reviewed by the appropriate staff;
  • corrective action plans are followed when PT results are found to be unacceptable or unsatisfactory;
  • quality assessment and quality control programs are established and maintained;
  • acceptable analytical test performance is established and maintained for each test system;
  • remedial actions are taken and documented when significant deviations from the laboratory’s established performance characteristics are identified, and patient test results are reported only when the system is functioning properly;
  • personnel have been appropriately trained and demonstrate competency prior to testing patient specimens
  • policies and procedures are established for monitoring personnel competency in all phases (preanalytic, analytic, and post-analytic) of testing to assure the ongoing competency of all individuals who perform testing;
  • remedial training or continuing education needs are identified, and training provided; and an approved procedure manual is available to all personnel.
  • Manage a team. Review and approve assigned work; mentor and develop personnel, including dedicated succession planning and contingency management.
  • This role works with PHI on a regular basis both in paper and electronic form and has an access to various technologies to access PHI (paper and electronic) in order to perform the job.
  • Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training and security training as soon as possible but not later than the first 30 days of hire.
  • Must maintain a current status on Natera training requirements.


  • Excellent written and oral communication skills.
  • Experience leading a laboratory offering prenatal screening and oncology testing and evaluating, interpreting, and reporting out NGS and microarray data.
  • Familiarity with next-generation sequencing, and/or knowledge of advanced methods of copy number detection.
  • Strong background in human and medical genetics, and oncology with a familiarity of online human genomics.
  • Understanding of statistical measures utilized in genetic testing and screening.


  • MD/DO degree and ABP board-certified/eligible in AP/CP and Molecular Genetic Pathology preferred.
  • Qualified for unrestricted Medical License to practice in the state of CA (current California Medical License holder preferred)
  • Qualified or Current Certificate of Qualification in Genetic Testing from the NYS CLEP required.
  • Five or more years of experience in a CLIA-certified clinical laboratory setting analyzing, interpreting and reporting clinical genetic/genomic data (fresh MGP fellowship graduates will be considered as well).
  • Knowledge of CAP, CLIA, California, and New York state regulations.
  • Management experience required.


  • Duties typically performed in BSL-2 lab setting.
  • Standing or sitting for long periods of time may be necessary.
  • Duties may require working various shifts, weekends, and/or overtime.

Travel required for this position:

No ☐ or Yes ☒ : If yes state anticipated percent for travel: up to 10%

Driven by the passion for elevating the science and utility of genetic testing, Natera is committed to helping families identify and manage genetic diseases. Natera is a rapidly-growing diagnostics company with proprietary bioinformatics and molecular technology for analyzing DNA. Our complex technology has been proven clinically and commercially in the prenatal testing space and we are actively researching its applications in the liquid biopsy space for developing products with oncology applications.
The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.
Competitive Benefits. Generous Employee Referral program. Healthy catered lunches everyday, and premium snacks! Additionally, we offer complimentary premium coffee drinks and teas, and other beverages. 
For more information, visit
Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.
All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.