The State Of eSource Adoption In Clinical Trials

As eSource adoption accelerates across clinical research, sites are becoming a critical factor in successful digital trial execution. Drawing on findings from Paradigm Health’s 2026 industry survey, this report examines how sponsors are evaluating site readiness, scaling hybrid data capture models, and addressing operational barriers that continue to slow broader implementation. The research highlights why eSource capability is increasingly influencing site selection decisions and how connected workflows can reduce manual entry, improve data quality, accelerate study timelines, and ease site burden. Readers will gain practical insight into the evolving expectations placed on research sites and the strategies sponsors and sites can use to operationalize eSource more effectively across future trials.