Candice Del Rio has over 16 years of clinical research experience (Phases I-III) across site, CRO, and sponsor settings in various therapeutic areas including oncology and infectious diseases. She has built operational infrastructure, led QMS validation, ensured HIPAA compliance, and configured EDC systems while also overseeing the

recruitment and onboarding of high-performing teams. Her expertise in

process optimization, SOP development, and compliance leadership

enhances efficiency and trial integrity. With a deep understanding of

stakeholder objectives in drug development, she ensures clinical excellence

while supporting the commercial success of innovative health technologies

and targeted therapies.