At the direction of the Clinical Trials Director, provides day-to-day project assistance with faculty research studies. Recruits, screens, and conducts the informed consent process with eligible research participants and tracks participation over time. Reviews health information from participants electronic medical records to screen for eligibility.Developing and maintaining research regulatory documentation including, but not limited to Institutional Review Board (IRB) submissions, amendments, and continuing reviews as well as study specific CRFs.Develops and provides, with supervision from Senior Research Program Coordinator, participant educational materials. Collects clinical data and maintains study databases and ensures data is complete and accurate.Uses a variety of software and database technologies, including REDCap, Excel, and other software and databases to enter data and track study activities. Enters all required study data on an ongoing basis. Participates in weekly study team meetings and regular trainings and in-services with the study team.Other related duties as assigned.