Michael Wayne

Background

About Michael Wayne

Michael Wayne is an experienced Quality Assurance Manager & Senior Clinical Research Associate with 10 years of clinical research experience and 2 years of bench research experience. He has a demonstrated history of working in a fast-paced clinical research environment as well as a proven history of overseeing efficient site management, verifying comprehensive and accurate study endpoint data, ensuring compliance with federal, local, and industry regulations, all while consistently meeting essential metrics & timelines. Michael has ensured quality control of clinical research data in support of multiple complex oncology research study protocols across multiple Phase I-IV disease indications that include Malignant Hematology, Solid Tumor Oncology, Neurology, and Internal Medicine. Additionally, he has conducted bench research with a focus in Endocrinology and Colorectal Cancer. Michael has completed comprehensive training designed at fostering success in research setting. He is highly knowledgeable and skilled in Site Management, Informed Consent, Serious Adverse Event reporting, protocol compliance, GCP, IATA DGR, CTCAE, RECIST, multiple Electronic Data Capture (EDC) systems, Institutional Review Board (IRB), Early-Development Clinical Oncology trials (Phase I), and Clinical Data Management.