Clinical Genomic Scientist – Curation

🔥 0 minutes ago

🇺🇸 United States – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👻 Ghost score 10%

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Baylor Genetics

WebsiteLinkedInAll Job Openings

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 data • Curate variants, genes, and gene-disease correlations following ACMG guidelines using internal datasets, online resources, and published literature • Analyze NGS, Sanger sequencing, metabolomics, and chromosomal microarray data • Select variants for curation or confirmation and apply HGVS nomenclature • Draft clinical reports for review • Document data-quality findings, variant evidence, source references, discrepancy resolution, and confirmation or repeat-analysis decisions • Escalate unexpected, discrepant, incomplete, or technically limited cases to qualified supervisory or clinical personnel • Support test validation and process refinement • Present findings at meetings • Maintain knowledge of genomic variation and its relationship to human disease • Apply data quality assessment principles • Monitor test turnaround time and delegate tasks as needed • Adhere to the Baylor Genetics Compliance Program Code of Conduct • Perform other duties as assigned

🎯 Requirements

• PhD or MD in clinical medicine, genetics, molecular biology, or equivalent; strong candidates with a Master’s degree and relevant experience, such as genetic counseling, will be considered • 0–2 years relevant experience in variant curation or clinical genomics; new graduate with Ph.D./M.D. or Master's with appropriate experience acceptable • 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 and communicating genetic details effectively • Excellence in reading and writing medical language • Proficiency in Microsoft Office (Excel, Word, PowerPoint, Outlook) • Expertise in ACMG/AMP variant interpretation • Clinical genetics and report writing experience • Literature review and evidence evaluation expertise • Familiarity with NGS workflows and sequencing data • Experience with ClinVar, OMIM, gnomAD, and HGMD • Knowledge of CAP/CLIA quality standards • Strong organizational, data quality, and prioritization skills • Strong communication and collaboration skills

🏖️ Benefits

• Remote work with daily huddles, clear objectives, and flexible scheduling • Occasional weekend rotation may be needed (for example, once a month) • Equal opportunity employer committed to fostering an inclusive and diverse workplace • Application-process accommodation support