Duties for this position include coordinating the initiation, management and completion of clinical research studies, performing a wide range of clinical and non-clinical tasks associated with conducting clinical research; collaborating with investigators and other team members to achieve research project objectives; ensuring data integrity and compliance with research protocols with the guidance of more senior research staff.   In addition, the Research Assistant will act as a liaison between investigators, sponsors, study subjects, Institutional Review Board, Contract Research Organizations, and ancillary services, and will adhere to U.S. Food and Drug Administration and International Conference on Harmonization regulations as well as individual study protocols.  Other duties, as assigned.