Maintain deep technical fluency in Fulgent's FulGenome whole genome analysis-covering SNVs, CNVs, genome-wide deletions and duplications, mitochondrial variants, and repeat expansions across 20,000+ genes in a single report-as well as TruPath Genome, which adds long-range insights for complex structural variants, repeat expansions, difficult-to-map regions, and phasing without parental samples. This role serves as a key scientific resource for external clinicians and internal teams, ensuring high-quality education and strategic communication with regards to Fulgent's pediatric rare disease genetic testing portfolio, including whole genome sequencing solutions such as FulGenome.