Job Description & How to Apply Below
Join the Clinical Laboratory team as a Senior Genomics Scientist at Stanford Health Care. This role emphasizes variant interpretation and molecular diagnostics in a collaborative environment.
In this senior-level position, you will work alongside laboratory directors, genetic counselors, and bioinformaticians. Your core responsibilities include prioritizing significant genetic variants and analyzing clinical sequencing data. You will also draft clinical reports and enhance diagnostic workflows, contributing to innovative molecular test designs and quality improvements.
Key Responsibilities:
• Identify clinically significant sequence variants using established tools
• Analyze published data for clinical case interpretations
• Classify and summarize significant genetic variants independently
• Enhance existing assays and develop new clinical-grade genetic tests
• Document quality improvements and participate in audits
Requirements:
• PhD or MS in Molecular Biology, Genetics, or related field
• 4+ years in genetics with CLIA certification
• 1+ year in diagnostic settings with NGS technology
• Experience evaluating genetic data and scientific literature
• Strong analytical skills with variant classification expertise
Leverage your scientific knowledge in genomics to impact patient care at Stanford Health Care.
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Position Requirements
10+ Years
work experience
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