Amanda Spratt, CCRP

Amanda Spratt, CCRP, has nearly eighteen years of experience in regulatory affairs and clinical cancer research. She is currently the technical director of the Cancer Clinical Trials Office (CCTO) at the University of Chicago Medicine Comprehensive Cancer Center (UCCCC) and, in that role, oversees regulatory compliance for adult oncology studies conducted at the University. She received a BS in Biology from Boston College before entering clinical research. She has extensive experience in regulatory affairs, including Institutional Review Board (IRB) requirements, good clinical practice guidelines, and the US Code of Federal regulations that govern clinical research activities. She has a detailed understanding of the framework of clinical cancer research, including protocol design and regulatory requirements of both clinical sites and commercial sponsors. Amanda is passionate about education and enjoys sharing her knowledge of the complex clinical trials regulatory environment with others.