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Clinical Genomics Variant Scientist

Ucla Health
UCLA Health
3-7 years
$105700-234500 Annually
10 Feb. 6, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Genomics Variant Scientist

Job ID: 27905
Employment Type: Full-Time, Permanent (Staff – Career)
Location: Los Angeles, California, United States
Work Schedule: Monday to Friday | 8:00 AM – 5:00 PM
Salary Range: USD 105,700 – 234,500 per annum
Posted Date: December 29, 2025
Organization: UCLA Health
Function: Molecular Diagnostics | Clinical Genomics | Precision Medicine


Role Overview

UCLA Health is seeking a highly skilled Clinical Genomics Variant Scientist to join its Molecular Diagnostics Laboratory. This role plays a critical part in precision medicine by curating, interpreting, and reporting germline and somatic genomic variants derived from high-complexity sequencing assays.

The position supports clinical diagnostics, test development, and translational research initiatives, working closely with clinicians, genetic counselors, and laboratory professionals to deliver accurate and clinically meaningful genomic insights.


Key Responsibilities

  • Review and interpret patient clinical information and next-generation sequencing (NGS) data from high-complexity assays, including:

    • Clinical Exome Sequencing

    • Solid Tumor Sequencing Panels

    • Hematologic Malignancy Sequencing Panels

  • Perform variant curation and classification using established guidelines (e.g., ACMG/AMP, AMP/ASCO/CAP) and evidence-based genomic resources

  • Prepare, review, and finalize high-quality clinical genomics reports, ensuring clarity, accuracy, and clinical relevance

  • Develop, maintain, and update standard operating procedures (SOPs) related to variant interpretation, classification, and reclassification workflows

  • Submit curated variants to public genomic databases such as ClinVar in compliance with best practices

  • Collaborate cross-functionally with molecular pathologists, genetic counselors, clinicians, and laboratory teams

  • Support test development, assay validation, quality improvement initiatives, and implementation of new molecular diagnostics

  • Contribute to clinical research projects aligned with precision medicine and translational genomics


Required Qualifications and Experience

Education

  • Master’s or Doctoral degree (MS, PhD, MD, or equivalent) in Genetics, Genomics, Molecular Biology, Bioinformatics, or a related life sciences discipline

Experience

  • Minimum 3–7 years of relevant experience in clinical genomics, molecular diagnostics, or variant interpretation within a clinical or CLIA-certified laboratory environment

  • Demonstrated experience interpreting germline and/or somatic variants from NGS-based assays

  • Experience with clinical reporting and variant classification frameworks


Key Skills and Competencies

  • Strong expertise in variant curation, interpretation, and clinical genomics reporting

  • Working knowledge of NGS technologies, cancer genomics, and inherited disease genomics

  • Familiarity with genomic databases and tools such as ClinVar, gnomAD, COSMIC, OMIM, and PubMed

  • Excellent scientific writing, documentation, and communication skills

  • Ability to work effectively in multidisciplinary clinical and research teams

  • High attention to detail, quality, and regulatory compliance

  • Understanding of laboratory quality standards, validation processes, and continuous improvement


Why Join UCLA Health

UCLA Health is a globally recognized leader in healthcare, research, and academic medicine. Joining the Molecular Diagnostics Laboratory offers the opportunity to work at the forefront of genomic medicine, contribute to impactful clinical care, and collaborate with experts shaping the future of precision diagnostics.


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