Isabel Chico-Calero, D.V.M., Ph.D., Regulatory Specialist, is responsible for providing assistance and guidance to investigators reporting results in the federal database ClinicalTrials.gov. She provides expert guidance on clinical trial registration and disclosure requirements such as FDAAA, ICMJE, CMS and NIH. In addition, she supports investigators holding investigational product applications from the FDA (IND/IDE). Isabel helps investigators achieve optimal conduct of human research in accordance with federal requirements and institutional policies through educational activities and consultations. Isabel has extensive experience as researcher in the fields of immuno-oncology, surgical and disease models, in vivo optical imaging, and host-pathogen molecular pathogenesis. She conducted her predoctoral research work in Europe and worked at MGH as postdoctoral research fellow prior to joining the QI Program. Isabel keeps her connection with the biomedical research community as an external consultant for preclinical studies.