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