David Hammond, MS, RAC, CCRP

Director, Quality & Regulatory Affairs

Dave provides direction to Curiex’s quality systems, GCP compliance, audit readiness, CAPA frameworks, and continuous improvement across all sites. With more than a 30 years in clinical quality and regulatory operations, Dave maintains deep institutional memory through his long-standing working relationship with Eric as a co-instructor in the University of Washington Masters and Certificate programs in clinical trials for more than two decades. In addition to Curiex, Dave serves as Associate Professor in the School of Pharmacy at the University of Washington focusing on Biomedical Regulatory Affairs and Clinical Research and Director of the BRAMS (Biomedical Regulatory Affairs MS) program and is the chair of an institutional review board, and serves as a consultant to several biotechnology companies, providing guidance on regulatory strategy, clinical trial design and operations, and compliance with the FDA and other regulatory bodies around the world. Dave holds a Regulatory Affairs Certification in Medical Devices (RAC), the Certified IRB Professional (CIP), the Certified Clinical Research Professional (CCRP) and a number of other industry certifications. He currently serves on the board of the Organization of Regulatory and Clinical Associates (ORCA) and was the inaugural recipient of the Martha Feldman Award for service and education to the regulatory community. He is also an alumnus of the UW BRAMS program.