Baylor Genetics
501 - 1000 employees
Founded 1978
🏥 Healthcare
💼 Consulting
🍽️ Food & Beverage
Healthcare • Consulting • Food & Beverage
Baylor Genetics is a clinical genomics and precision diagnostics laboratory affiliated with Baylor College of Medicine that provides comprehensive genetic testing and interpretation services. The company offers whole genome and whole exome sequencing, chromosomal microarray analysis, mitochondrial testing, pharmacogenomics, and specialized assays, along with genetic counseling, provider support, and insurance/payment resources. Baylor Genetics supports healthcare providers, researchers, and families with AI-enhanced interpretation, multimodal data integration, and end-to-end clinical and laboratory services.
Clinical Genomic Scientist – WGS
🔥 0 minutes ago
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Baylor Genetics
501 - 1000 employees
Founded 1978
🏥 Healthcare
💼 Consulting
🍽️ Food & Beverage
Healthcare • Consulting • Food & Beverage
Baylor Genetics is a clinical genomics and precision diagnostics laboratory affiliated with Baylor College of Medicine that provides comprehensive genetic testing and interpretation services. The company offers whole genome and whole exome sequencing, chromosomal microarray analysis, mitochondrial testing, pharmacogenomics, and specialized assays, along with genetic counseling, provider support, and insurance/payment resources. Baylor Genetics supports healthcare providers, researchers, and families with AI-enhanced interpretation, multimodal data integration, and end-to-end clinical and laboratory services.
📋 Description
• Analyze clinical genetics and genomics data • Curate variants, genes, and gene-disease correlations following ACMG guidelines • Select variants for curation and confirmation • Apply HGVS guidelines for variant nomenclature • Summarize findings for clinical reports • Assist laboratory directors and R&D with validation of cutting-edge technologies and software platforms • Draft clinical reports • Support test validation and process refinement • Present findings • Monitor test turnaround time • Delegate tasks • Participate in virtual meetings
🎯 Requirements
• PhD or MD in clinical medicine, genetics, molecular biology, or equivalent • Alternatively, a Master’s degree and relevant experience may qualify • 2–4 years of variant curation experience • Familiarity with American College of Medical Genetics (ACMG) variant curation guidelines • Knowledge of genomic variation and its correlation with human disease • Expertise in clinical medicine, genetics, genomics, or molecular biology • Experience in data quality assessment • Ability to communicate genetic details effectively • Excellence in reading and writing medical language • Proficiency in Microsoft Office (Excel, Word, PowerPoint, Outlook) • Experience in bioinformatics analysis, variant effect prediction algorithms, and scripting languages desired • Preferred MB(ASCP) certification • Experience with independent variant interpretation • Experience with complex case review and phenotype correlation • Experience with multi-gene panel and exome interpretation • Advanced literature review and evidence assessment • Knowledge of SOPs, CAP, and CLIA standards • Discrepancy resolution and consensus review participation • Clinical reporting and communication skills • Cross-functional collaboration skills
🏖️ Benefits
• Remote work arrangement • Equal opportunity and inclusive workplace • Accommodation during the application process • Occasional weekend rotation may be needed (for example, once a month)
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