Brandon Keith
Clinical Research Program Director- Department of Ophthalmology @University of Colorado Anschutz
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WORK HISTORY
Clinical Research Program Director- Department of Ophthalmology @University of Colorado Anschutz
Denver, CO, US
Provide strategic leadership and operational management for the Department of Ophthalmology clinical trials program, directing program planning and growth.·Oversee the full lifecycle of sponsored and investigator-initiated ophthalmology studies, including feasibility, start-up, patient recruitment, study execution, and close-out.·Lead and direct clinical research teams, regulatory and research staff, promoting high-quality study conduct, professional development, and adherence to institutional policies and quality standards.·Ensure regulatory and institutional compliance, maintaining adherence to FDA regulations, ICH-GCP guidelines, and IRB requirements while coordinating with research and regulatory offices at the University of Colorado Anschutz Medical Campus.·Manage program partnerships and financial operations, including sponsor and CRO relationships, clinical trial budgets and contracts, and identification of new research opportunities to expand the department’s clinical trials portfolio.
EDUCATION
University of South Florida
Graduate Certificate in College Teaching, Higher Education/Higher Education Administration
University of South Florida
Bachelor of Arts - BA, Political Science and Government
University of South Florida
Graduate Certificate in Public Health, Public Health
University of South Florida
Master of Arts (M.A.), American Studies/Political Science
ABOUT BRANDON KEITH
Proven research leader with 20+ years of strategic and operational experience in clinical trial programs, regulatory compliance, and research administration across academic, nonprofit, and private clinical settings. Extensive experience supporting pre-clinical and clinical research programs, including ophthalmology and oncology trials. Strong record of building high-performing research teams and operational infrastructure supporting compliant, efficient research programs. Collaborates with investigators, sponsors, and institutional stakeholders to advance patient-centered research while expanding clinical trial portfolios.
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