Investigator Budgets' Impact on Patient Enrollment and Retention: How to Improve Sponsor/CRO/Site Selection Processes
Track
:
Track 01: Clinical Operations
Program Code:
241
Date:
Tuesday, June 26, 2012
Time:
1:30 PM to 3:00 PM
EST
CHAIR
:
Daniel Ulrey, Midwest Clinical Support, Inc., United States
Dan Ulrey is Co Founder, President and CEO of Midwest Clinical Support, Incorporated, a site network of 391 independent investigative sites with experience in 128 disease states in all phases of clinical development.
As the Chief Operating Officer for CenterWatch, Joan is responsible for the business operations, financial performance, marketing, and sales of the company along with setting strategic direction. Joan's work experience includes: CHI, Tufts CSDD at Tufts University, Thomson CenterWatch, & PAREXEL.
Debby Brown, ICON Clinical Research, United States
As VP, Cardiovascular, Metabolic Disease, Pain & Inflammatory Disease at PharmaNet/i3, she is responsible for the oversight & conduct of global clinical trials within these 2 therapeutic areas. She has +20 years experience in the management & oversight of clinical trials.
Description
Study budgets and site identification and selection processes continue to result in study timelines being extended and a significant loss of experienced investigators. Senior executives from industry will discuss how identification and selection processes can be improved as well as how to achieve real fair market value in site study budgets and payment terms. These methods and processes continue to cause a dramatic reduction in the number of GCP-qualified US-based investigators and have dramatically extended study timelines and added significant cost to Pharma, resulting in severe Pharma employee reductions and cost shifting of R&D expense to CROs. It remains to be seen if this strategy will result in increased productivity.
Learning Objectives: Discuss how study budgets are formulated and developed and how they can be improved Explain how sites can be better identified and selected Describe how the processes for site identification and selection can be improved with Pharma and CROs.