Clinical Genomic Variant Analyst - Remote

Overview

The Clinical Genomic Variant Analyst will interpret genetic sequence variations identified through diagnostic clinical genetic testing, focusing on gene panels and exome analysis performed by Next Generation Sequencing (NGS). This role is part of a vibrant scientific community committed to understanding human genetic variation.

In Short

• Perform interpretation of genetic sequence variations.
• Use NGS analysis software for patient genetic data.
• Evaluate gene relevance to diseases.
• Support molecular diagnostic lab activities.
• Participate in drafting clinical reports.
• Mentor analysis staff and collaborators.
• Assist in scientific writing and presentations.
• Train new personnel.
• Collaborate with research laboratories.
• Perform related work as needed.

Requirements

• PhD in a related field required.
• 2-5 years of relevant work experience.
• Strong background in human genetics and NGS.
• Experience in rare disease analysis.
• Familiarity with genomic tools and databases.
• Ability to interpret scientific literature.
• Preferred programming and bioinformatics skills.
• Excellent communication skills.
• Strong organizational skills.
• Ability to work collaboratively in a team.

Benefits

• Comprehensive health benefits.
• Retirement plans.
• Paid time off.
• Professional development opportunities.
• Supportive work environment.
• Collaboration with leading researchers.
• Mentorship opportunities.
• Participation in conferences.
• Inclusive workplace culture.
• Access to university resources.