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Genomic Variant Analyst Jobs (NOW HIRING)

(Associate) Scientist, Health Data

Seattle, WA · On-site

$67K - $67K/yr

Variant Bio is developing life-saving therapies by studying the genes of people with exceptional ... Genomic study-design literacy: Able to recognize when recruitment, sampling, batching, or ...

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ABOUT THE ROLE The Health Data team at Variant Bio turns data generated in the field, across our ... Genomic study-design literacy: Able to recognize when recruitment, sampling, batching, or ...

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Genomic Variant Analyst information

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$38K

$73.5K

$117.5K

How much do genomic variant analyst jobs pay per year?

As of Jul 15, 2026, the average yearly pay for genomic variant analyst in the United States is $73,532.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,000.00 and $79,500.00 per year, depending on experience, location, and employer.

What does a Genomic Variant Analyst do?

A Genomic Variant Analyst is a specialist who examines genetic data to identify and interpret variations within genomes, such as mutations or structural changes in DNA. Their work is crucial for understanding genetic contributions to diseases, guiding clinical decision-making, and advancing personalized medicine. They use bioinformatics tools and databases to analyze sequencing data, annotate variants, and assess their significance. Genomic Variant Analysts often collaborate with clinicians, researchers, and laboratory staff to ensure accurate and meaningful interpretation of genomic information.

What are the key skills and qualifications needed to thrive as a Genomic Variant Analyst, and why are they important?

To thrive as a Genomic Variant Analyst, you need a strong background in genetics, molecular biology, and bioinformatics, typically supported by a relevant degree such as in genomics or computational biology. Experience with genomic data analysis tools (like GATK, VEP, or IGV), next-generation sequencing (NGS) platforms, and familiarity with databases such as ClinVar are essential. Attention to detail, problem-solving skills, and effective communication are important soft skills for interpreting results and collaborating with multidisciplinary teams. These capabilities ensure accurate variant identification, meaningful clinical interpretations, and successful integration of genomic data into research or healthcare.

What are some common challenges faced by Genomic Variant Analysts when interpreting complex genetic data, and how are they addressed?

Genomic Variant Analysts often encounter challenges such as distinguishing between benign and pathogenic variants, managing large volumes of sequencing data, and staying updated with rapidly evolving databases and guidelines. To address these, analysts rely on established variant classification frameworks, utilize collaborative review with clinical teams, and leverage specialized bioinformatics tools. Continuous professional development and participation in case discussions help ensure accurate interpretations and effective collaboration with genetic counselors and physicians.

How to become a genome analyst?

To become a genomic variant analyst, typically a bachelor's degree in genetics, biology, bioinformatics, or a related field is required, often followed by specialized training or a master's degree. Skills in data analysis, programming languages like Python or R, and experience with genomic databases and tools are essential. Certifications in bioinformatics or genomics can enhance job prospects, and familiarity with laboratory techniques and sequencing technologies is beneficial.

What is the highest paying job in genetics?

In genetics, roles such as genetic counselors, clinical geneticists, and research directors tend to have the highest salaries, often exceeding $150,000 annually. Senior positions requiring advanced degrees, certifications, and extensive experience typically command the highest compensation in the field.

What does a variant analyst do?

A genomic variant analyst examines genetic data to identify and interpret variations in DNA sequences that may be linked to diseases or traits. They use bioinformatics tools, databases, and statistical methods to analyze sequencing data, often working with next-generation sequencing technologies and requiring attention to detail and knowledge of genetics. Their work supports research, diagnostics, and personalized medicine efforts.

What does a genomic analyst do?

A genomic analyst studies genetic data to identify variations and mutations that may impact health or disease. They analyze DNA sequences using bioinformatics tools, interpret results, and often work in research or clinical laboratories, requiring knowledge of genetics, programming, and data analysis. Their work supports diagnostics, personalized medicine, and genetic research.

What is the difference between Genomic Variant Analyst vs Bioinformatics Technician?

AspectGenomic Variant AnalystBioinformatics Technician
Required CredentialsBachelor's or Master's in Genetics, Bioinformatics, or related field; experience with genomic data analysisAssociate's or Bachelor's in Bioinformatics, Computer Science, or related field; basic scripting skills
Work EnvironmentLaboratories, research institutions, biotech companiesResearch labs, hospitals, biotech firms, computational environments
Employer & Industry UsageGenomics research, clinical labs, pharmaceutical companiesData processing, supporting genomic research, data management

The Genomic Variant Analyst focuses on interpreting genetic variations and analyzing sequencing data, often requiring advanced bioinformatics skills. In contrast, the Bioinformatics Technician typically handles data management, basic analysis, and supporting research activities. While both roles work within genomics and bioinformatics, the analyst role involves more complex data interpretation and analysis, whereas the technician provides essential support functions.

More about Genomic Variant Analyst jobs
What cities are hiring for Genomic Variant Analyst jobs? Cities with the most Genomic Variant Analyst job openings:
What states have the most Genomic Variant Analyst jobs? States with the most job openings for Genomic Variant Analyst jobs include:
What job categories do people searching Genomic Variant Analyst jobs look for? The top searched job categories for Genomic Variant Analyst jobs are:
Infographic showing various Genomic Variant Analyst job openings in the United States as of July 2026, with employment types broken down into 94% Full Time, and 6% Part Time. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $73,532 per year, or $35.4 per hour.
Staff Scientist - Integrative Genomics Core

Staff Scientist - Integrative Genomics Core

City of Hope

Duarte, CA

Full-time

Posted 8 days ago


City Of Hope rating

8.4

Company rating: 8.4 out of 10

Based on 88 frontline employees who took The Breakroom Quiz

27th of 885 rated healthcare providers


Job description

Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.

We are seeking an experienced and highly motivated Staff Scientist to join the Integrative Genomics Core. You will provide scientific leadership in the development, optimization, and execution of advanced genomics workflows. You will work closely with investigators to design experiments, implement new technologies, and ensure delivery of high-quality sequencing data. You will also contribute to strategic growth of the core by evaluating and deploying emerging genomics platforms and methodologies.

The Integrative Genomics Core provides comprehensive genomics services to support cutting-edge biomedical research. Leveraging advanced platforms such as Illumina, PacBio, Nanopore, and 10x Genomics, the core enables a broad range of genomic and epigenomic applications. These technologies empower investigators to explore complex biological systems, from cancer genomics to translational and precision medicine studies, within a highly collaborative, service-oriented environment.

As a successful candidate, you will:

·         Provide design and consultation on genomic approaches with investigators, including study design, sample requirements, and technology selection

·         Complete complex genomics workflows such as bulk, single-cell, and long-read sequencing applications

·         Develop, optimize, and update current protocols for Illumina, PacBio, Nanopore, and 10x Genomics platforms

·         Evaluate and implement emerging technologies to expand core capabilities

·         Ensure quality control standards and best practices across all stages of sample processing and sequencing

·         Communicate results to investigators; collaborate with bioinformatics teams on data analysis as needed

·         Assist with grant applications, methods development, and collaborative publications where appropriate

·         Train, mentor, and provide technical guidance to research staff and junior personnel

Your qualifications should include:

·         Ph.D. in Genomics, Molecular Biology, Genetics, or a related field

·         Minimum 3-5 years’ experience in genomics or sequencing technologies

·         Extensive hands-on experience across multiple sequencing platforms, including Illumina, PacBio, and 10x Genomics

·         Expertise Expertise in library preparation for a variety of applications (RNA-seq, DNA-seq, ATAC-seq, ChIP-seq/CUT&RUN, methylation assays, and long-read sequencing); experience with single-cell and/or spatial genomics workflows (e.g., 10x Genomics Chromium, Visium)

·         Strong understanding of genomics applications, including transcriptomics, epigenomics, and variant analysis

·         Experience working in a core facility or shared resource environment with a strong service orientation

·         Ability to develop, optimize, and validate wet-lab protocols and implement new technologies

·         Demonstrated ability to troubleshoot complex experimental issues and improve workflow efficiency

·         Strong mentoring and training experience for junior staff in laboratory techniques and best practices

·         Excellent communication skills with experience consulting with investigators on experimental design and sample requirements

·         Experience supporting collaborative research projects and contributing to methods sections of manuscripts or grants

City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.

City of Hope is an equal opportunity employer.  

To learn more about our Comprehensive Benefits, please CLICK HERE.


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About City of Hope

Sourced by ZipRecruiter

City of Hope is an independent biomedical research and treatment organization for cancer, diabetes and other life-threatening diseases. Founded in 1913, City of Hope is a leader in bone marrow transplantation and immunotherapy such as CAR T cell therapy. City of Hopes translational research and personalized treatment protocols advance care throughout the world. Human synthetic insulin, monoclonal antibodies and numerous breakthrough cancer drugs are based on technology developed at the institution. AccessHope, a subsidiary launched in 2019 serves employers and their health care partners by providing access to City of Hopes specialized cancer expertise. City of Hope is ranked among the nations Best Hospitals in cancer by U.S. News & World Report and received Magnet Recognition from the American Nurses Credentialing Center. Its main campus is located near Los Angeles, with additional locations throughout Southern California and in Arizona.

Industry

Hospitals

Company size

1,001 - 5,000 Employees

Headquarters location

Duarte, CA, US

Year founded

1913