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PRA Experts to Present at DIA Annual Conference
Date:6/20/2012

RALEIGH, N.C., June 20, 2012 /PRNewswire/ -- PRA, a leading Clinical Research Organization, announces that two of our experts will speak at the DIA 48th Annual Meeting being held in Philadelphia from 24-28 June.

On 25 June at 3:30PM EDT, Gretchen Goller, Senior Director of PRA's Patient Access and Recruitment Services (PARS) group will deliver a speech titled "Setting Sites Up for Success in the New Digital Environment." Her discussion will focus on key elements of success for establishing and supporting clinical trial sites in today's digital world.

Ms. Goller joined PRA in 2011 and has over 15 years of clinical research experience. She began her career as a study coordinator and then became a site director at the University of Pennsylvania. Most recently, Ms. Goller served as a patient recruitment and retention strategist at a pharmaceutical company, where her focus was on Phase II-IV clinical studies. At PRA, Ms. Goller has assumed a leadership role in the PARS group and works with our strategists to implement recruitment and retention programs on all pertinent studies. 

On 26 June at 1:30PM EDT, Kathleen Mandziuk, Senior Scientific Affairs Director of PRA's Late Phase Service (LPS) group, will co-lead an interactive session titled, "Non-interventional Minimal Risk Research: A 360-degree Perspective." The discussion will focus on minimal risk research strategies and feature perspectives from a range of industry experts. Specifically, Ms. Mandziuk will focus on the impact of observational/non-interventional research on sponsors, CROs, physicians and patients. Other presenters include Linda Coleman, Director of Regulatory Affairs and General Counsel at Quorum IRB and Winifred Meeker-O'Connell from the Department of Health and Human Services at the FDA.

Ms. Mandziuk has extensive experience in strategic design and implementation of observational and late phase studies and has directed all operational aspects of these
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