We are seeking an exceptional candidate to drive the genomic analysis of electronic medical records (EMRs). You will be developing and applying innovative machine learning and data science approaches to combine genomic information with routine health-care data to uncover relationships in human biology and disease. You will help to build up knowledge of the systems, ontologies and use practices of EMRs across health care systems that are engaged in large-scale genomic data collection. You will lead the development of digital phenotyping approaches for establishing robust clinical interpretation that capture primary disease and features such as disease subtype, progression and response to treatment. You will work with statisticians to develop approaches for the genetic interpretation of disease phenotypes obtained from EMR, combining information on both common and rare genetic variation. You will be passionate about the opportunity of genetics to transform healthcare.