Clinical Genomics Analyst: Variant Interpretation

Belay Diagnostics; Chicago (IL); On-site; USD 65,000 - 90,000; Full time

Job summary

Belay Diagnostics is seeking a Clinical Genomic Analyst to support clinical testing by interpreting somatic and cfDNA variants, generating clear reports, and performing QC within a regulated lab setting in the Midwest. The role involves collaboration with multidisciplinary teams and adherence to privacy and compliance standards.

The successful candidate will have at least 1 year of genomic interpretation experience, strong molecular genetics knowledge, and proven written and verbal communication

Qualifications

• Must have a minimum of 1 year of understanding or working with genomic variant interpretation.
• Strong foundations in molecular genetic technology principles.
• Excellent written and verbal communications skills.
• Work successfully in a multidisciplinary team environment.
• Prior experience in regulated laboratory environment (e.g. CLIA, CAP) is preferred.

Responsibilities

• Interpret somatic and cfDNA sequence variants to determine clinical significance.
• Evaluate variant function and genotype-phenotype relationships using literature and tools.
• Write clear, communicable reports based on test results.
• Perform quality control of variant analyses, interpretations and reports.
• Troubleshoot technical issues and assist in resolution per lab policies.
• Assist in development, evaluation, and implementation of new procedures.
• Maintain safety records and ensure compliance with established protocols.
• Review and revise SOPs as needed and requested by supervisor.
• Maintain effective communication within the department and with external professionals.
• Maintain a positive attitude when faced with challenges.

Skills

Genomic variant interpretation

Molecular genetics principles

Written communication

Verbal communication

Team collaboration

CLIA/CAP experience

Job description

Belay Diagnostics is seeking a Clinical Genomic Analyst to support clinical testing by interpreting somatic and cfDNA variants, generating clear reports, and performing QC within a regulated lab setting in the Midwest. The role involves collaboration with multidisciplinary teams and adherence to privacy and compliance standards.

The successful candidate will have at least 1 year of genomic interpretation experience, strong molecular genetics knowledge, and proven written and verbal communication