Maxine Koepp, JD

Ms. Koepp assists with development of the study protocol, procedures, and implementation.

Ms. Koepp is a Protocol Coordinator at the Clinical Trials Statistical Data Management Center in the College of Public Health at the University of Iowa. She has over 26 years of experience in clinical trials, including drug and device trials, in industry, contract research organizations, and academia. As the Protocol Coordinator for the FM TIPS Study, she participates in protocol development, the drafting of data collection tools, database development and design, Institutional Review Board submissions and compliance, and assists clinical sites in assuring protocol compliance combined with data completeness and accuracy.