Coordinate and implement several complex research projects in the form of day-to-day management and operations of research projects. Develop and maintain project plans and/or the other tools to track deliverables and ensure successful completion of project. Pro-actively identify and resolve issues related to projects. Complete all study start-up needs such as obtaining study materials from sponsor and ensuring regulatory documents are completed through internal processes. Managing project close-out activities. Perform subject visits for study activities including identification and screening of potential participants, consenting, enrollment, scheduling, study drug and study device dissemination and accountability, and all study visit procedures. Complete all data collection, sample processing and study monitoring visits. Coordinate logistics of meetings and capturing minutes from meeting. Coordinate with other departments, schools at the University and partner institutions. Actively participate in research meetings and events. Assist in the specialized clerical and technical duties connected with human subject research and other administrative tasks as assigned.Responsible for clinical communications with sponsors, central and local IRBs, vendors, monitors, and investigators. Assist with the data management, analysis, and results reporting. Determining data collection standards according to study outcomes, maintaining and monitoring standards for data collection, developing templates to ensure consistency with specific standards.Identify and respond to research-related adverse events.Other related duties as assigned.