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Baylor Genetics

Clinical Genomic Scientist II – Clinical Indication

Baylor Genetics

Clinical Genomic Scientist II analyzing clinical genetics data and curating variants at Baylor Genetics. Collaborating with lab directors on cutting-edge technologies and clinical reports.

Posted 7/24/2026full-timeRemote • 🇺🇸 United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

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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

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Applicant Tracking System Keywords

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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.