A full-time Research Study Assistant is needed to support complex research projects under the direction of the clinical research manager by recruiting, screening, consenting, and scheduling study participants. This individual creates and maintains study files, tracks subject visits, and maintains and monitors regulatory compliance. This position requires effective communication with clinicians and other project personnel, including members of other laboratories both internal and external to BU/BMC. This position will also be responsible for processing biospecimens for storage. This position will support ongoing IRB protocols including subject recruitment and enrollment, subject bio sample collection and processing, and entering clinical data into the established data management system (REDCap).