Michelle A. Detry is a Director, Adaptive Trial Execution & Senior Statistical Scientist for Berry Consultants with expertise in Phase I, II, and III clinical trial design and analysis/reporting in support of Data Monitoring Committees (DMCs). She received her PhD in Biometry in 2003 from the University of Texas-Houston School of Public Health. Prior to joining Berry Consultants in 2011, Dr. Detry was an Assistant Scientist in the Department of Biostatistics & Medical Informatics in the University of Wisconsin School of Medicine and Public Health. In that role, she led projects focused on the design and creation of reports prepared for independent DMCs for multicenter Phase II/III and Phase III industry sponsored clinical trials, frequently taught seminars on study design and statistical methods to postdoctoral clinical fellows, and co-developed the workshop series “Clinical Research Study Design”. Prior to her position at the University of Wisconsin, Michelle was a Principal Statistical Analyst at the University of Texas M. D. Anderson Cancer where she designed clinical trials using Bayesian methods. In addition to clinical trials, Dr. Detry has experience in the analysis of data for healthcare quality improvement, epidemiology, and basic science research.