Genomic Variant Scientist I
The Women’s Health and Genetics division of LabCorp is seeking a Variant Scientist to join our Variant Science Group (VSG) team. This position will perform technical and non-technical analysis to classify DNA sequence variants from high complexity genetic testing according to established standard operating procedures and protocols. Utilizes internal data, bioinformatics tools, and published resources to classify variants identified through sequencing assays into designated classification categories. Performs gene-disease association curation according to established protocols.
Please note: this is a 100% remote position. Candidate can be located anywhere in the US.
The schedule for this position will be Monday - Friday, 8am-5pm local time zone.
Responsibilities:
Processes and classifies DNA sequence variants and/or DNA Copy Number Variants (CNVs) identified through sequencing platforms in accordance with company SOPs
Utilizes in-house rule-based classification workbench to evaluate and score variants for classification
Employs bioinformatics tools and resources to aid in variant classification
Performs search of published literature and databases as needed for each variant classified
Carefully curates content in variant classification worksheets in a traceable and concise manner
Upon completion of classification, exports report for review by reporting directors and genetic counselors to support external client requests
Performs gene-disease association curation according with company protocols
Researches and interprets variants from whole exome or whole genome sequencing and assesses their clinical relevance by correlating findings with clinical information
Maintains tracking documents in relation to the variant classification
Ensures that variants are classified in adherence to established rules of HGVS nomenclature
Ensures that variants are classified in a timely manner in accordance with production timelines
Ensures required communication regarding variant classification is performed in a timely manner
Participates in variant scientist team discussions and meeting
Attends scientific meetings of relevance to the department and company when required
Requirements:
PhD in Life Sciences (Genetics, Molecular Biology or Biological fields) or Master’s in Genetic Counseling required
Minimum 1 year of experience in classifying variants based on ACMG guidelines in a clinical setting required
A strong background in Human Genetics as well as familiarity with human mutation databases and HGVS nomenclature is required
Strong analytical capabilities, scientific writing and communication skills, organization, and the ability to critically review, comprehend, ascertain and document relevant clinical and functional data from scientific publications and online databases
Ability to use bioinformatics software and Microsoft Office suite of products (specifically use of Microsoft Excel to mine, parse and automate analysis of datasets)
Proficiency with large NGS datasets, in-silico tools, HGVS nomenclature, and genome browsers
Ability to meet production timelines with a sense of urgency and ethical responsibility in a rapidly evolving dynamic setting
Application Window Closes: 12/4/2025
**Salary Range: $81,000 - $120,000 / year
All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data.
Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here.
Labcorp is proud to be an Equal Opportunity Employer:
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
We encourage all to apply
If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.
About the job
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Genomic Variant Scientist I
The Women’s Health and Genetics division of LabCorp is seeking a Variant Scientist to join our Variant Science Group (VSG) team. This position will perform technical and non-technical analysis to classify DNA sequence variants from high complexity genetic testing according to established standard operating procedures and protocols. Utilizes internal data, bioinformatics tools, and published resources to classify variants identified through sequencing assays into designated classification categories. Performs gene-disease association curation according to established protocols.
Please note: this is a 100% remote position. Candidate can be located anywhere in the US.
The schedule for this position will be Monday - Friday, 8am-5pm local time zone.
Responsibilities:
Processes and classifies DNA sequence variants and/or DNA Copy Number Variants (CNVs) identified through sequencing platforms in accordance with company SOPs
Utilizes in-house rule-based classification workbench to evaluate and score variants for classification
Employs bioinformatics tools and resources to aid in variant classification
Performs search of published literature and databases as needed for each variant classified
Carefully curates content in variant classification worksheets in a traceable and concise manner
Upon completion of classification, exports report for review by reporting directors and genetic counselors to support external client requests
Performs gene-disease association curation according with company protocols
Researches and interprets variants from whole exome or whole genome sequencing and assesses their clinical relevance by correlating findings with clinical information
Maintains tracking documents in relation to the variant classification
Ensures that variants are classified in adherence to established rules of HGVS nomenclature
Ensures that variants are classified in a timely manner in accordance with production timelines
Ensures required communication regarding variant classification is performed in a timely manner
Participates in variant scientist team discussions and meeting
Attends scientific meetings of relevance to the department and company when required
Requirements:
PhD in Life Sciences (Genetics, Molecular Biology or Biological fields) or Master’s in Genetic Counseling required
Minimum 1 year of experience in classifying variants based on ACMG guidelines in a clinical setting required
A strong background in Human Genetics as well as familiarity with human mutation databases and HGVS nomenclature is required
Strong analytical capabilities, scientific writing and communication skills, organization, and the ability to critically review, comprehend, ascertain and document relevant clinical and functional data from scientific publications and online databases
Ability to use bioinformatics software and Microsoft Office suite of products (specifically use of Microsoft Excel to mine, parse and automate analysis of datasets)
Proficiency with large NGS datasets, in-silico tools, HGVS nomenclature, and genome browsers
Ability to meet production timelines with a sense of urgency and ethical responsibility in a rapidly evolving dynamic setting
Application Window Closes: 12/4/2025
**Salary Range: $81,000 - $120,000 / year
All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data.
Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here.
Labcorp is proud to be an Equal Opportunity Employer:
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
We encourage all to apply
If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.
