CHAIR
:
SPEAKER
(S):
Mary Jo Lamberti, PhD,MA (SPKSUP), Senior Project Manager, Tufts Center for the Study of Drug Development, Tufts University, United States
Leslie(Mi Ok) Chong, MA (SPKNON), Senior Clinical Program Leader, Genentech, A Member of the Roche Group, United States
Shyla VanReenen,
(SPKNON), Senior Manager, Clinical Operations,
Synteract, Inc., United States
Shyla has been in the clinical research industry for about 20 years, starting as a study coordinator, moving to a CRA role, and for the last 12 years working in project and clinical management within the CRO sector. Most recently, she has started to grow a study feasibility group.
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Description
This symposium will examine key metrics within the clinical trial initiation process, and the first presentation will present the results of aggregate company data. Data from studies completed during 2008-2011 were analyzed across study and site level. A second presentation will examine those strategies and approaches that drive efficiencies during study startup including protocol review, targeted site identification and streamlined regulatory document collection. The third presentation will examine various solutions to conduct efficient investigator meetings.