Kathleen Caldwell, AS, CCRP
Associate Director
Development Strategy & Compliance
Kathleen is a seasoned clinical research leader with over 20 years of experience in biomedical research and more than nine years of focused expertise in ophthalmology. As Associate Director of Strategic Development & Compliance, Kathleen plays a key role in advancing research strategy, infrastructure, and regulatory alignment in support of complex clinical trials.
With a strong foundation in genetics, systems design, and team productivity, Kathleen has held progressive roles at OIRRC, including Senior Project Manager. Prior to joining OIRRC, Kathleen coordinated ophthalmology research at the University of Nebraska Medical Center, where earlier work also included contributions to teratogen studies in maternal-fetal medicine.
Kathleen brings more than six years of experience in management and is especially skilled in organizational planning, systems infrastructure, and team leadership. This cross-functional background is central to enhancing clinical trial efficiency and regulatory readiness.