Event Date/Time: Oct 11, 2012 End Date/Time: Oct 12, 2012
Early Registration Date: Sep 07, 2012
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This in-depth, two-day program will feature case studies, lessons learned and presentations focused on the challenges associated with role-based training in the clinical research environment. Included are strategies for linking training initiatives to study outcomes, key regulatory considerations and findings, and examples of how training deficiencies can put clinical research activities at risk.

Featured presentations include:

Maximizing Training Resources Across Clinical Research Job Functions with Herb Anthony, Associate Director, Clinical and R&D Training, MedImmune, Inc.

Optimizing CRA Training: Case Studies, Lessons Learned and Examples with Danielle Hoskins, Senior Manager, CMR Training, Novo Nordisk, Inc.

Clinical Research Training for Global Teams with Cathy Ollom, RN, BSN, OCN Global Training and Education, Sarah Cannon Research Institute and Maribeth Johnson, CCRP Research Educator, Sarah Cannon Research Institute

“iReady”: Design and Methodology in Online Trainings to Ensure Engagement, Fun and Learning Transfer with Gerlinde Jayme, Head, Continuous Learning & Development, Global Clinical Operations, EMD Serono and Cécile Nicolas-Denizou, Global Training Manager, Continuous Learning & Development, Merck Serono

Creating and Deploying a Good Clinical Practices (GCP) Program for Clinical Research Professionals at a Large Medical Device Company with Catherine Russell, RN, BSN, Senior Clinical Quality Training Specialist, Global Clinical Operations, Medtronic, Inc.

Also taking place at the summit are three timely programs on Clinical Protocol Development, Virtual Investigator Meeting Management, and Clinical Project Management and Clinical Training and new for 2012, four tactical short courses.

For event updates and to register, visit http://bit.ly/2012CTR (barnettclinicalsummit.com)


Additional Information

Secure your place by September 7, 2012 to receive advance registration discount.