Clinical Genomics Scientist – Report Writing

🕒 August 4

🇺🇸 United States – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✏️ Content Writer

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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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

• Curate variants, genes, and gene-disease correlations following ACMG guidelines • Analyze clinical genomics data • Select variants for curation or confirmation • Apply HGVS guidelines for variant nomenclature • Draft clinical reports • Support test validation and process refinement • Present findings • Monitor test turnaround time • Assist laboratory directors and R&D with validation of technologies and software platforms

🎯 Requirements

• Board-certified Genetic Counselor preferred, or PhD/MD in clinical medicine, genetics, molecular biology, or a related field • For Genetic Counselors: minimum three years of patient-facing genetic counseling, including test ordering, clinical documentation, patient-resource development, report interpretation, and communication of complex results • 2–4 years of experience in clinical genomics or related fields, including postdoctoral appointments • Thorough understanding of 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, including Excel, Word, PowerPoint, and Outlook • Preferred PhD or better in Molecular Cell Sciences • Desired experience in bioinformatics analysis, variant effect prediction algorithms, and scripting languages • Ability to curate variants, genes, and gene-disease correlations • Knowledge of HGVS variant nomenclature guidelines

🏖️ Benefits

• Remote work from a home office • Occasional weekend rotation may be needed (for example, once a month) • Equal opportunity and inclusive, diverse workforce commitment