About the Role We are seeking a highly motivated Genomics Research Scientist to drive research and translational applications in precision health and precision medicine. This role focuses on extracting clinically and biologically meaningful insights from Next Generation Sequencing (NGS) and large-scale genomic datasets, bridging genomics, computational analysis, and medical decision-making. You will work closely with clinicians, data scientists, and domain experts to translate genomic variation into actionable insights that inform disease risk assessment, diagnosis, and personalized treatment strategies. Key Responsibilities Precision Medicine . Analyze and interpret Whole Genome Sequencing (WGS) and Whole Exome Sequencing (WES) data . Identify, annotate, and prioritize genetic variants relevant to human disease . Associate variant effects with disease phenotypes using: o Current medical and genomic literature o Public and proprietary variant databases . Generate high-quality gene sequencing reports that: o Clearly communicate variant significance o Support clinical decision-making by physicians . Collaborate with clinicians to refine interpretation frameworks and reporting standards Precision Health . Perform Polygenic Risk Score (PRS) analysis for complex diseases . Apply PRS methods to population-scale genomic datasets . Integrate PRS with Electronic Health Records (EHR) to: o Refine disease risk prediction o Improve stratification for specific conditions . Evaluate and validate PRS performance across cohorts and disease indications
