Clinical Genomic Scientist – Report Writing

🔥 12 hours ago

🇺🇸 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

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

🎯 Requirements

• PhD or MD in clinical medicine, genetics, molecular biology or equivalent required; or a Master’s degree and relevant experience for strong candidates • 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 and communicating 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 skills • Data quality and analytical skills • Knowledge of SOPs, CAP, and CLIA standards • Discrepancy resolution and consensus review participation • Clinical reporting and communication skills • Cross-functional collaboration skills

🏖️ Benefits

• Equal opportunity and inclusive workplace commitment • Accommodation during the application process • Remote work arrangement • Occasional weekend rotation may be needed, for example once a month