QA and Regulatory Compliance Associate

Liz joined the Clinical Quality Management Program in 2020. Her primary focus is promoting clinical research quality and compliance through the development of policies and processes within the CQMP central office as well as tools, checklists, and educational opportunities to aid Quality Management Reviewers during the monitoring process.  Liz has an extensive and varied background in clinical research having spent 14 years with the Duke Cancer Institute (DCI) as a site coordinator, a clinical data manager for cooperative research, and a senior CRA/monitor for DCI’s single and multi-site investigator initiated trials.