Christine Pierre (Society for Clinical Research Sites)
Matthew Roe (Duke Clinical Research Institute)
Panel members sharing their perspectives on these recommendations include:
David Ciavarella (C.R. Bard)
Robin Douglas (QuintilesIMS)
Terri Hinkley (Academy of Medical-Surgical Nurses)
Kaitlin Malone (Amgen)
Webinar Objective
Attendees will learn how:
Workload, reporting burdens, time allocation challenges, and financial issues contribute to high rates of investigator turnover;
Investigators and study staff can benefit from improvements to research infrastructure and training and educational opportunities;
All stakeholders can contribute to optimizing trial conduct and to developing more efficient and transparent approaches to budgeting and contracting; and
Investigators can connect with opportunities to remain engaged in clinical research.
*CTTI encourages the use of all materials listed on this site in the pursuit of improving the clinical trials enterprise. If you use any of the slides from this presentation, please let us know, credit CTTI, and make it clear that you are not presenting on behalf of CTTI.