Clinical Genomic Scientist II – Clinical Indication

🔥 9 minutes ago

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Baylor Genetics

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 1978

🧬 Biotechnology

🔬 Science

Biotechnology • Science

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

• The Clinical Genomics Scientist II analyzes clinical genetics data, curates variants and genes, and summarizes findings for clinical reports. • Our scientists assist laboratory directors and R&D with validation of cutting-edge technologies and software platforms. • Curation (50%): curation of variants, genes, and gene-disease correlation following ACMG guidelines. • Analysis (30%): analyzing clinical genomics data, selecting variants for curation/confirmation, variant nomenclature following HGVS guidelines. • Other (20%): may involve clinical report drafting, test validation, process refinement, presenting findings, monitoring test turnaround time and task delegation.

🎯 Requirements

• Required PhD or MD in clinical medicine, genetics, molecular biology or equivalent. • Or Strong candidates with a Master’s degree and relevant experience. • 2-4 years of variant curation experience. • Preferred MB(ASCP) certification. • Familiarity with American College of Medical Genetics (ACMG) variant curation guidelines. • Knowledge of genomic variation and its correlation with human disease. • Expertise in concepts of 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).

🏖️ Benefits

• EEO STATEMENT Baylor Genetics is proud to be an equal opportunity employer committed to fostering an inclusive and diverse workplace. We welcome and encourage applicants from all backgrounds to apply.