Julie Holub, MBA, CCRP, has worked in clinical research for over 15 years. Initially working as a research assistant, Julie has held numerous positions in research operations and research compliance. In her current role, her focus is on facilitating FDA regulated, investigator-initiated research, and supporting commercial collaborative partnerships between Academic Medical Centers and industry partners. Julie has expertise in protocol development, research operations, regulatory compliance, as well as project and data management throughout the clinical trial life cycle.