Liz will assist the Director of Study Operations of the NeuroNEXT Clinical Coordination Center (CCC), work closely with the NeuroNEXT Central IRB (cIRB) to develop policies and procedures and with all cIRB staff to manage site cIRB submissions. She will also assist with site management and support under the direction of the Director of Site Management and will be a member of the Intervention Team, and other NeuroNEXT committees as needed. Liz has over 20 years of experience in drug, device and biologic clinical research including clinical trial coordination, study monitoring and project management of multi-center trials in academic and industry settings. She is dedicated to the NeuroNEXT collaboration and will participate in the NeuroNEXT-CCC Leadership Team and will assist with cIRB coordination, CCC site management and all NeuroNEXT site activities as needed, to help facilitate the network objective of improving clinical trial quality and efficiency.