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Clinical Genomic Scientist II – Clinical Indication
Baylor GeneticsClinical Genomic Scientist II analyzing clinical genetics data and curating variants at Baylor Genetics. Collaborating with lab directors on cutting-edge technologies and clinical reports.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical genomics, including variant curation and analysis, while adhering to ACMG and HGVS guidelines. Proficient in drafting clinical reports and communicating complex genetic information effectively.
Highest-signal resume keywords
Variant Curation ExperienceACMG Guidelines FamiliarityClinical Report DraftingData Quality AssessmentPhD Or MD In Clinical Medicine
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Variant CurationClinical Genomics Data AnalysisGene-Disease CorrelationVariant NomenclatureGenomic Variation Knowledge
Soft Skills
Effective CommunicationTask Delegation
Tools & Technologies
Microsoft OfficeExcelWordPowerPointOutlook
Certifications & Qualifications
MB(ASCP) Certification
Industry Keywords
Clinical GeneticsMolecular BiologyGeneticsGenomicsACMG Guidelines
About the role
Key responsibilities & impact- 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
What you’ll need- 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
Comp & perks- 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.