Position Summary: Provide study coordination related to research and clinical trial activity as defined by the department’s Policies and Procedures. Job Specific Duties and Responsibilities: Assure all study requirements are documented and meet both internal and external regulations in accordance with protocol guidelines. Update the Clinical Trials Management System (CTMS). Activate trials in accordance with institutional guidelines. Manage submission of study documentation to the required regulatory agencies.  Coordinate and conduct trial activities including data maintenance and research subject interfacing. Serve as project liaisons to other departments, outside organizations