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Join Us for Our Seminar »
Optimizing Study Design and Protocol Development
Today's clinical trials are more complex than ever before. But do they have to be? Recent research indicates that up to a quarter of all procedures conducted during a clinical trial aren't associated with any of the study's key objectives or endpoints, accounting for at least a fifth of a trial's per patient procedure costs.
We invite you to join this seminar to hear industry thought leaders share their experiences and discuss how these issues can be addressed. This seminar will enable you to:
- Get the details of the latest research on study design and protocol development;
- Hear from your peers on their efforts to streamline their study design processes and simplify their protocols;
- Learn what you can do to minimize the time and money your organization spends on activities that don't impact your studies' key objectives; and
- Understand the role that structured study design and improved line of sight can have in optimizing your study execution.
Seminar Details
Date:
Wednesday, December 11, 2013 |
Time:
9:00 am-1:30 pm ET |
Location:
Bridgewater Marriott
700 Commons Way
Bridgewater, NJ 08807
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Agenda:
- Registration & Breakfast
9:00 - 9:30 am
- Introductions:
9:30 - 9:40 am
- Trends & Challenges in Study Design
9:40 - 10:30 am
- Sponsor Perspective
10:30 - 11:00 am
- Break
11:00 - 11:15 am
- Change-Management
Approach for Optimizing
Study Design
11:00 - 11:15 am
- Study Design Optimization:
The Right Tools, Better Data
and Streamlined Processes
11: 45 - 12:15 pm
- Panel Discussion
12:15-12:45 pm
- Lunch & Networking
12:45 - 1:30 pm
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Participants
- Ken Getz
Director, Sponsored Research Programs, Associate
Tufts University School of Medicine
- Joseph Drost
Senior Consultant
ER Squared, Inc.
- Jason Attanucci
National Director, Study and Protocol Design
Medidata Solutions
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