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Entry Level Variant Curation Scientist Jobs (NOW HIRING)

... Scientists ... Assists with the day-to-day operations of variant assessment, curation, and documentation to ...

ExpertScientific Literacy - Ability to critically read, interpret, and apply findings from scientific literature to clinical practice and variant curation. * Communication & Knowledge Sharing ...

... Scientists. Assists with the day-to-day operations of variant assessment, curation, and documentation to accurately identify and classify genomic alterations detected through genomic testing and ...

... Entry-Level Variant Education & Experience Bachelors degree in Business, Life Sciences, Engineering, or a related field OR Associate degree or relevant medical/clinical certification (CST, RN, RT, PT ...

... of fundamental scientific discoveries to improve human health locally and around the globe ... Genomic alignment and variant curation. * Maintain and curate project databases in collaboration ...

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Entry Level Variant Curation Scientist information

What are the key skills and qualifications needed to thrive as an Entry Level Variant Curation Scientist, and why are they important?

To thrive as an Entry Level Variant Curation Scientist, you need a solid background in genetics, molecular biology, and data analysis, usually supported by a bachelor’s or master’s degree in a relevant field. Familiarity with bioinformatics tools, genomic databases (such as ClinVar or gnomAD), and variant interpretation guidelines (like ACMG/AMP) is essential. Attention to detail, critical thinking, and strong written communication are important soft skills for accurately interpreting and reporting genetic variants. These skills ensure accurate variant classification, which is crucial for supporting clinical decision-making and advancing genomic medicine.

What are some typical challenges faced by entry level variant curation scientists when interpreting genetic data?

As an entry level variant curation scientist, you may encounter challenges such as distinguishing between benign and pathogenic genetic variants, dealing with ambiguous or limited scientific literature, and ensuring accurate data annotation. You will often need to collaborate closely with senior scientists, genetic counselors, and clinicians to clarify findings and make informed decisions. Developing strong critical thinking skills and staying current with evolving guidelines and databases are essential for overcoming these challenges and building expertise in the field.

What is an Entry Level Variant Curation Scientist?

An Entry Level Variant Curation Scientist is a professional who analyzes genetic data to determine the clinical significance of genetic variants. They review scientific literature, databases, and laboratory findings to classify genetic mutations as benign, pathogenic, or of uncertain significance. Their work supports genetic testing, diagnosis, and personalized medicine by ensuring accurate interpretation of genetic information. Entry level roles typically require a background in genetics, biology, or related fields, and involve training in data analysis and variant interpretation.

What is the difference between Entry Level Variant Curation Scientist vs Entry Level Bioinformatics Analyst?

AspectEntry Level Variant Curation ScientistEntry Level Bioinformatics Analyst
Required CredentialsBachelor's in Genetics, Biology, or related field; knowledge of genetic variantsBachelor's in Bioinformatics, Computer Science, or related field; programming skills
Work EnvironmentLaboratories, research institutions, biotech companiesData analysis, research labs, healthcare organizations
Industry UsageGenomics, personalized medicine, genetic testingHealthcare, research, biotech

While both roles involve data analysis and genetic information, the Entry Level Variant Curation Scientist focuses on evaluating and annotating genetic variants, whereas the Entry Level Bioinformatics Analyst primarily analyzes large datasets using computational tools. The former emphasizes genetic knowledge, while the latter emphasizes programming and data management skills.

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Infographic showing various Entry Level Variant Curation Scientist job openings in the United States as of May 2026, with employment types broken down into 79% Full Time, and 21% Part Time. Highlights an 71% In-person, and 29% Remote job distribution.
Clinical Genomics Variant Scientist

Clinical Genomics Variant Scientist

UCLA Health

Los Angeles, CA

$105.70K - $234.50K/yr

Full-time

Posted 2 days ago


UCLA Health rating

8.7

Company rating: 8.7 out of 10

Based on 133 frontline employees who took The Breakroom Quiz

6th of 864 rated healthcare providers


Job description

Description

The Molecular Diagnostics Laboratory is seeking an experienced Variant Scientist to join our clinical team. In this critical role, you will curate and interpret germline and somatic variants and prepare high-quality clinical reports derived from exome and targeted cancer sequencing assays. You will contribute to variant classification, test development efforts, and clinical research projects that advance precision medicine for patients across UCLA Health and beyond. Primary duties include:

• Review and assess patient clinical notes and sequencing data from high-complexity molecular assays, including Clinical Exome Sequencing, Solid Tumor Sequencing Panels, and Hematologic Malignancy Sequencing Panels.

• Perform variant curation and interpretation using established guidelines and evidence-based resources.

• Draft and refine clinical reports, ensuring accuracy, clarity, and clinical relevance.

• Develop and update SOPs for variant curation, interpretation, and reclassification workflows

• Participate in submitting curated variants to public databases (e.g. ClinVar) and contribute to quality improvement and test development initiatives.

• Collaborate with clinicians, genetic counselors, and laboratory staff to support accurate and timely reporting.

• Contribute to clinical research projects and assist in implementing new molecular diagnostic assays.

Salary Range: $105,700.00 - $234,500.00/year 

Qualifications
• At least two years’ experience in germline variant curation is required. Somatic variant curation experience is a plus.
• Strong working knowledge of laboratory genetics and genomics, including target capture, amplification, and massively parallel sequencing.
• Familiarity with widely used genomic tools such as IGV and UCSC/COSMIC genome browsers
• Ability to establish effective working relationships with clinicians, genetic counselors, and other team members.
• Programming or bioinformatics experience (e.g. R, SAS, Perl, Python, regex, database design) – preferred.
• PhD in human genetics, molecular genetics, cancer biology, or a related discipline – preferred. Master’s degree in molecular biology, genetics, or a closely related field may be considered with relevant experience.


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About UCLA Health

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UCLA Health, operating within the healthcare industry, is significantly recognized for its commitment to improving the health and wellbeing of people through the integration of patient care, research, and education. Located in Los Angeles, California, UCLA Health was founded and associated with the University of California, Los Angeles (UCLA) in 1955, entrenching its roots in quality healthcare service provision. Through a broad range of medical services, UCLA Health significantly stands as a cornerstone for comprehensive outpatient, inpatient, and emergency care services, specialized treatments, and wellness checks. Notable for pioneering an integrated, comprehensive medical approach, UCLA Health is consistently ranked among the top health systems in the US and world.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Los Angeles, CA, US

Year founded

1955