Clinical Genomic Variant Scientist – US

About the job

Clinical Genomic Variant Scientist

Variantyx provides cutting-edge diagnostic tools coupled with cross company teamwork to foster a meaningful and exciting career applying genomic medicine to diagnose patients with rare disease. For more than 7 years Variantyx has established itself as the industry leader in clinical genomic sequencing and interpretation as the first diagnostic lab to provide a comprehensive clinically validated whole genome test that includes structural variation, short tandem repeats, and large and small chromosomal abnormalities from a single base to the whole chromosome.

Position Summary

As a Clinical Variant Scientist located in the US or Israel, you will be responsible for the interpretation and analysis of genetic variants that are identified by our Genomic Intelligence® platform.

Responsibilities:

Your duties will include interpreting sequence variants in the context of genetic disorders, curating medical and molecular literature, and compiling clinical draft reports.

Requirements:

• Process and classify variants in accordance with company SOPs
• Consult with the Laboratory Directors, Genetic Counselors or Technical team members regarding variant assessment
• Communicate with customers and peers within the company
• Provide feedback for product enhancement

Testing Personnel:

A person competent to record and report test results promptly, accurately, and proficiently, and for assuring compliance with applicable regulations.

Qualifications:

• Applicants must possess a PhD in Molecular Biology or Genetics, or alternatively, an MSc/MS in Genetic Counseling, Molecular Biology, Genetics, or Bioinformatics. Candidates with a BS/BSc in a relevant field will also be considered if accompanied by a minimum of 2 years of experience in variant analysis and interpretation.
• At least 5 years’ experience working in a clinical diagnostic genetic lab using NGS testing and ACMG variant scoring.
• Experience with NGS analysis is required