Track Clinical Trial Agreement execution status at each site and coordinate with participating sites'' research administration offices Maintain the regulatory binder/eRegulatory system: protocol versions, informed consent forms, IRB approvals and amendments, training records, and delegation logs Track participant enrollment progress at each site against targets Perform direct data collection responsibilities for the lead site Coordinate device and supply logistics to participating sites (fitting kits, tape supplies, recording devices, prescription lens orders) Support internal and external reporting, including sponsor progress reports Contribute to results dissemination, including manuscript and conference preparation support Grant reporting Grant preparation and submission for future projects Identification of new clinical trial site opportunities for the practice. Clinical Trial Project Management Duties (Primary Focus) Assist the Principal Investigator in the overall day-to-day management of the multicenter trial Coordinate patient recruitment and enrollment activities across all participating sites Track protocol adherence across sites and help resolve protocol deviations Coordinate the schedule of study visits and monitor enrollment/visit-completion timelines against the study''s schedule of events Manage data transfer between participating sites and the coordinating site, and support preparation of data for analysis Prepare and maintain data collection instruments Assist with regulatory approvals, IRB reliance/authorization agreements, and clinical trial registration (e.g., ClinicalTrials.gov)