As artificial intelligence (AI) becomes an inescapable fact of daily life, in this interactive session, attendees will obtain a basic understanding of how AI has been used in clinical research to date and what it may make possible in the future.

CEU: 1.00 ACRP

Speakers:

• Jeff Sidell, Chief Technology Officer, Advarra

• Wendy Tate, PhD, Director of Advanced Analytics and Research Optimization, Advarra

Watch a Sneak Peek into the Session Content:

The urgency to revolutionize the process by which sponsors assess a study site's feasibility for handling a clinical trials has never been more apparent. This session considers how, as trial volumes surge and staffing shortages loom, the frustrations shared by sponsors, contract research organizations (CROs), and sites alike underscore the need for innovative approaches to data collection and site selection that will lead to successful trials.

CEU: 1.00 ACRP

Speakers:

• Andrea Bastek, PhD, VP of Innovation, Florence Healthcare

• Amy Bland, Director of Clinical Research, Baptist Health Institute for Research and Innovation

• Victor Chen, Managing Director, Clinical Trials Program, Kaiser Permanente

• Nancy Sacco, PhD, VP Head of Clinical and Site Development Operations, SiteBridge Research Inc

Related Blog Content:

• Fixing Feasibility: Collaborative Approaches for Redefining and Improving Site Selection

Watch a Sneak Peek into the Session Content:

This session offers a U.S. Food and Drug Administration Investigator's insights from sponsor inspections that will help you to identify and prevent the problems that may arise for your data and/or application during the collection of tens to hundreds of thousands of documents during a single trial.

CEU: 1.00 ACRP

Speaker:

Lakecha Lewis, International Inspection Cadre, U.S. Food and Drug Administration

Watch a Sneak Peek into the Session Content:

This session will evaluate clinical trial operations at the site level and provide novel approaches for improving operations while providing effective oversight. These approaches will include redefining the roles of research team members to help retain quality professionals on board, from coordinators to principal investigators and everyone in between.

CEU: 1.00 ACRP

Speakers:

• Lacey Andrews, MS, CCRC, CCRA, Lead Clinical Research Coordinator, Marshall University's Joan C. Edwards School of Medicine, Department of Family and Community Health

• Todd Davies, PhD, Associate Director of Research, Joan C. Edwards School of Medicine

Participants in research are too often viewed as passive recipients rather than active members in the research process with individualized needs and personal views. This session focuses on how all members of the clinical trials team can improve participants’ experiences through a better understanding of participant-centric care in research, leading to increased engagement through recruitment and retention, and to more medical advances being available to the public sooner.

CEU: 1.00 ACRP

Speaker:

Kimberly Smith, Clinical Research Education Specialist, Tampa General Hospital

Watch a Sneak Peek into the Session Content

Connect with your colleagues and 100+ leading-edge organizations and suppliers helping you get better results in clinical research.

Relax and unwind with a beverage and light hors d'oeuvres at our reception beginning at 5:00pm.