The Clinical Research Coordinator is responsible for all aspects of pediatric clinical trials from feasibility to study close out. The CRC may provide support for multiple research studies within the divisions of Pediatric Gastroenterology, Hepatology and Nutrition, Infectious Diseases, and/or the Center for Development Behavior and Genetics. Diverse duties include implementing standards for research protocols in compliance with regulatory, institutional and external agencies, obtaining and organizing study data, assisting with IRB applications, submission and report writing, communication with study sponsor, coordination of site visits and study monitoring, and support for principal investigators with research projects, as needed. Will also be involved in screening for potential subjects and enrollments. Associate's degree and three years related experience or equivalent combination of education and experience required. Working knowledge of medical terminology, basic computer skills and good written/oral communication and organizational skills required. Experience with clinical research protocols preferred.