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Optimizing Protocol Data Collection to Reduce Site and Patient Participation Burden
Session Chair(s)
Kenneth Getz, MBA
Tufts Center for the Study of Drug Development
Tufts University School of Medicine, United States
This session presents results of a recent TransCelerate–Tufts CSDD study highlighting trends, benchmarking protocol data collection practices, and offering new, practical strategies to simplify protocol designs and reduce participant and site burden.
Learning Objective : Analyze new benchmarks on the distribution of protocol data across core, standard, and non-core endpoints; Identify procedures associated with non-core and non-essential endpoints and their contribution to patient and site burden; Discuss strategies to evaluate protocol data collection, simplify design and lower participation burden.
Speaker(s)
Frameworks and Tools Guiding Optimization of Protocol Data Collection
Jacqueline Cole, MS
Gilead Sciences, United States
Director, Design and Innovation, Clinical Operations
New Benchmarks on Clinical Trial Data Collection Practices and their Impact
Kenneth Getz, MBA
Tufts University School of Medicine, United States
Tufts Center for the Study of Drug Development
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