Stanford Health Care
The Genomics Sr Staff Scientist at Stanford Health Care collaborates with a multidisciplinary clinical laboratory team to interpret and prioritize clinically significant genetic variants from sequencing data. The role involves evaluating variant relevance using established guidelines, drafting clinical reports, and contributing to the development and validation of new molecular diagnostic tests. This position requires strong analytical skills and expertise in clinical genetics to support prompt patient care.
Headquarters
Palo Alto, California, United States
Company Size
10001+ employees
Founded
1885
Stanford Health Care is an academic, nonprofit medical center in Palo Alto that delivers the highest levels of care and compassion as part of Stanford Medicine. SHC treats a broad range of conditions—from cancer, heart disease, and brain disorders to primary care—offering specialty clinics, surgical services, and access to clinical trials. Known for multidisciplinary expertise and advanced, technology‑driven treatments, it operates Stanford Hospital and a network of outpatient centers across the Bay Area. Patients and referring providers choose SHC for complex, high‑acuity care informed by leading research and medical education.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Stanford Health Care.
Medical Scientist (Variant Curator) - Diagnostic Genomics, Pathology Services
Monash Health
Clinical Genomics Variant Scientist
Manatal
Variant Interpretation Scientist
Sequence Bio
Genome Analyst - Molecular Genetics
Commonwealth of Kentucky
Clinical Genomics Scientist
Baylor Genetics
Clinical Genomics Scientist
Baylor Genetics