Clinical Genomics Scientist, Oncology

Ph.D. in Human Genetics, M.S. in Genetic Counseling, or related field 2+ years of experience in somatic variant interpretation based on ACMG/AMP guidelines in a clinical setting Hands-on experience with human mutation databases (COSMIC, ClinVar, OncoKB), functional annotation sources (dbSNP), and genome browsers (UCSC) Familiarity with IGV and BAM file analysis Knowledge of cancer somatic mutation and signaling pathways Exceptional attention to detail and strong organizational skills Excellent communication skills and ability to work collaboratively

Perform somatic-based variant interpretation and data review Draft clinical reports using in-house reporting API Develop and modify somatic interpretation SOPs Contribute to curation of gene-level content Serve as a subject matter expert and present in molecular tumor boards Assist R&D team with somatic oncology projects