Clinical Genomics Variant Scientist

Amerit Consulting; United States; Remote; USD 60,000 - 80,000; Full time

Job summary

Amerit Consulting is seeking a Clinical Genomics Variant Scientist to support clinical diagnostics in hematological malignancies. This remote position involves interpreting somatic variants using next-generation sequencing data and writing clinical genomic reports while collaborating with a multidisciplinary team. A Ph.D. or M.S. in a relevant field and experience in somatic variant interpretation are required.

Benefits

Laptop will be provided

Qualifications

• Hands-on experience interpreting somatic variants.
• Proficiency in analyzing NGS data.
• Experience in drafting clinical genomic reports.

Responsibilities

• Curate and classify somatic variants identified through NGS assays.
• Draft clinical reports with genomic interpretations.
• Collaborate with cross-functional teams for clinical diagnostics.

Skills

Communication

Genomic Interpretation

Data Analysis

Education

Ph.D. or M.S. in Human Genetics, Molecular Biology, or related field

Tools

NGS Data Analysis Tools (ClinVar, COSMIC, gnomAD, etc.)

Bioinformatics Software

Job description

This range is provided by Amerit Consulting. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$65.00/hr - $75.00/hr

Direct message the job poster from Amerit Consulting

Recruiting Manager/ Lead Engineering Recruiter at Amerit Consulting

Position: Clinical Genomics Variant Scientist

Location: REMOTE

Duration: ~6 Month contract with a possible extension

Pay Rate: $65/hr – $75/hr (Depending on experience)

NOTE: Laptop will be provided

Position Overview

Manager seeking a Variant Scientist to support clinical diagnostics in hematological malignancies. The ideal candidate will have hands-on experience interpreting somatic variants using next-generation sequencing (NGS) data and drafting clinical genomic reports. This role involves working closely with a multidisciplinary team, including molecular biologists, pathologists, and bioinformatics engineers.

Key Responsibilities

• Curate and classify somatic variants identified through in-house hematologic malignancy NGS assays
• Draft clinical reports with accurate and relevant genomic interpretations
• Collaborate with cross-functional teams to support clinical diagnostics
• Troubleshoot challenges in data analysis and apply genomic expertise to clinical cases

Required Qualifications

• Ph.D. or M.S. in Human Genetics, Molecular Biology, Cancer Cell Biology, Genetic Counseling, Molecular Pathology, Medical Pharmacology, or a related field
• Demonstrated experience in somatic variant interpretation specific to hematologic cancers
• Proficiency in analyzing NGS data and using tools/databases such as ClinVar, COSMIC, gnomAD, VarSome, OncoKB, etc.
• Strong communication and writing skills
• Familiarity with laboratory genetics and genomics techniques (e.g., target capture, massively parallel sequencing)
• Ability to work independently and troubleshoot technical issues related to bioinformatics and IT platforms (Windows, MS Office, Zoom, VPN)

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Research and Science

• Industries

  Education and Biotechnology Research

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