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Sites, CROs, and Sponsor Relationship Obstacles and Opportunities
Program Code:
377
Date:
Wednesday, June 27, 2012
Time:
3:30 PM to 5:00 PM
EST
CHAIR
:
With 15+ yrs experience in the clinical research industry including study coordination, monitoring, & study management, Ms Collins has contributed to the development of Trifecta’s technical solutions that enhance the conduct of clinical research for the sponsor, site personnel, and CRAs.
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PRESENTER
(S):
With 15+ yrs experience in the clinical research industry including study coordination, monitoring, & study management, Ms Collins has contributed to the development of Trifecta’s technical solutions that enhance the conduct of clinical research for the sponsor, site personnel, and CRAs.
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Marie Smed,
Technical University of Denmark, Denmark
Researcher of innovation management focusing on pharmaceutical product development processes. In spring 2011 I had the pleasure of being a visiting researcher at TUFT CSDD under the guidance of Kenneth Getz. Kenneth Getz and I together conducted the study, which is presented at the DIA 2012 meeting.
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Rikki Hansen Bouchard has over 25 years of pharmaceutical development experience. She has held positions with two of the world's largest contract research organizations RH Bouchard & Associates, Inc. offers the services of thirty-seven consultants in 3 countries.
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Description
In this symposium, prerecorded interviews from site personnel will be a backdrop for discussions on how evolving sponsor/CRO relationships have affected sites, if the current paradigm is allowing sites to transfer their knowledge gained during clinical trials effectively, what sites ultimately need from the sponsor and CRO to consistently produce valuable data.
Learning Objectives:
Discuss key considerations when building a site, sponsor, and CRO relationship
Describe best practices regarding CROs, sites and sponsors
Identify questions that should be asked of sites before, during, and after the study.