JOB SUMMARY
The Clinical Genomics Scientist I 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. Position supports remote work with daily huddles, clear
objectives, and flexible scheduling.
KEY RESPONSIBILITIES
• Curate variants, genes, and gene-disease correlations following ACMG
guidelines using internal dataset, online resources, and published literature
• Analyze clinical genomics data including NGS, Sanger sequencing, metabolomics,
and chromosomal microarray; select variants for curation/confirmation; apply
HGVS nomenclature
• Draft clinical reports for review
• Document data-quality findings, variant evidence, source references,
discrepancy resolution, and required confirmation or repeat-analysis decisions
in the case record.
• Escalate unexpected, discrepant, incomplete, or technically limited cases to
qualified supervisory or clinical personnel before final report review.
• Support test validation, process refinement, and present findings at meetings
• Maintain knowledge of genomic variation and its relationship to human disease
• Apply data quality assessment principles
• Adhere to Code of Conduct per Baylor Genetics Compliance Program
• Perform other duties as assigned
KEY DUTIES & TIME ALLOCATION
• Curation (50%): curation of variants, genes, and gene-disease correlation
following ACMG guidelines.
• Analysis (30%): analyzing clinical genomics data, selecting variants for
curation/confirmation, and 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.
QUALIFICATIONS
Required
• PhD or MD in clinical medicine, genetics, molecular biology, or equivalent. Or
strong candidates with a Master’s degree and relevant experience, such as
genetic counseling, and relevant experience 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.
COMPETENCIES
• 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).
PHYSICAL DEMANDS AND WORK ENVIRONMENT
• Frequently required to sit, using a screen, keyboard, and mouse.
• Punctuality in attending virtual meetings.
• Occasional weekend rotation may be needed (for example, once a month).
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. We do not discriminate on the basis of
race, color, religion, national origin, sex, sexual orientation, gender
identity, age, veteran status, disability, genetic information, pregnancy,
childbirth, or any other status protected by applicable federal, state, or local
law. If you need an accommodation during the application process, please contact
our Human Resources team.