This session will focus on a high-impact site management model that addresses the critical industry gap whereby only 3% of physicians participate in clinical research. The presenter will demonstrate a comprehensive Sub-Investigator Training Checklist for transforming clinical practitioners into research-competent leaders who can assume authority and accountability for the ethical conduct of a study.

The core of the checklist's success lies in a "Physician-First Informed Consent" approach: by ensuring sub-investigators are expertly trained in critical trial-related procedures, they are equipped to relay protocol intricacies directly to their established patient base. This established trust ensures participants are not only enrolled but remain deeply engaged throughout the study lifecycle. The evidence-based methodology that utilized this training framework to achieve a sustained 98.9% participant retention rate will be discussed, providing attendees with a scalable blueprint for bridging the gap between clinical practice and research excellence.

CEU: 1.0 ACRP

Speaker:

• Khutaija Noor, MBBS, FCR, Clinical Research Lead, Amicis Clinical Trials