Tech Stack

Description

You will support day-to-day commercial reporting operations by performing somatic variant interpretation, drafting clinical reports using an in-house API, and contributing to oncology R&D projects. This role offers the opportunity to scale up reporting needs in a fast-paced entrepreneurial environment while improving patient care through clear clinical reporting.

Requirements

• PhD in Human Genetics, MS in Genetic Counseling, or related field
• 2+ years somatic variant interpretation experience using ACMG/AMP guidelines in clinical setting
• Hands-on experience with human mutation databases (COSMIC, ClinVar, OncoKB), dbSNP, UCSC browser
• Familiarity with IGV and BAM file analysis; willingness to learn basic bioinformatics tools
• Knowledge of cancer somatic mutations, signaling pathways, and FDA-approved drugs

Responsibilities

• Perform somatic-based variant interpretation with BAM file analysis
• Draft clinical reports using in-house reporting API
• Contribute to curation of gene-level content (domain, critical residues)
• Work closely with R&D team on oncology projects providing variant interpretation expertise
• Support engineering and QA teams on reporting and language