Tracey Nardi-Zimmer

Tracey Nardi-Zimmer has a strong background in clinical research and regulatory affairs. Tracey has held various positions ranging from Clinical Research Assistant to Protocol and Site Feasibility Manager. Their responsibilities have included coordinating trial meetings, ensuring regulatory compliance, and managing trial master files. With experience in both industry-sponsored and cooperative group trials, Tracey has a proven track record of maintaining documentation and ensuring audit readiness.