Research sites often juggle multiple sponsor-required technology systems across their studies. This patchwork of systems can lead to duplicative data entry, repeated training, and inefficient workflows that add significant administrative burden to already demanding workloads.
This session will introduce a new AI-powered ChatGPT-like experience for protocol and study document review, and how using site-preferred systems—including the electronic medical record (EMR) and clinical trial management system (CTMS)—can help researchers and coordinators work more efficiently in sponsor-led trials. We will discuss workflows that integrate with existing systems and explore how greater flexibility in technology choices can reduce duplicate work and streamline daily study tasks.
Attendees will gain a practical understanding of how Bring Your Own Technology BYOT approaches are evolving across the clinical research ecosystem and how leveraging familiar systems can simplify study operations.
This session does not provide ACRP Contact Hours.
Speaker:
Keith Wright, Sr. Director, Strategy, Advarra
