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Register today and join your peers and colleagues!

 

Barnett International & Cambridge Healthtech Institute’s Second Annual Mastering Clinical Trial Monitoring will focus exclusively on the changing role and expanding expectations of the clinical trial monitor. Building on the overwhelming success of last year’s inaugural event, monitoring thought leaders will present best practices, strategies, and techniques for the experienced monitor. Sessions will be focused on improving the monitor’s job performance, and improving site performance through monitoring. We will also feature perspectives on FDA activities, and how monitoring is affected by recent inspection trends. Themes throughout will include tools and techniques, monitoring in electronic environments, global monitoring challenges, and monitoring in special circumstances. Attendees can expect case studies, hands-on activities, takeaway tools, and interactivity. 

Join CRA's (Clinical Research Associates), Site Monitors, Clinical Affairs and More!

FINAL AGENDA

Key Areas to be Addressed:

• Strategic Site Monitoring and Risk Management
• Managing and Improving Site Relationships
• Improving Site Performance
• Monitoring Medical Device Studies
• Monitoring in Special Environments
• Improving Efficiency with Technology
• Monitoring Leadership Development

 

Featured speakers:

Nancy Bakke, Principal, Clinical Study Manager, Clinical Research Monitor, Sorin CRM, USA, Inc. Alana Chenault, Clinical Operations Lead – Oncology, US Clinical Operations, inVentiv Clinical Solutions, on Assignment with Pfizer Worldwide Research and Development John Creech, CCRP, Clinical Research Associate, Clinical Operations, Abbott Vascular Angelia Drake, RN, Surgical Oncology, Baylor Health Care System Keri-Ann Heck-Winters, RN, BSN, CCRA, CCRC, Clinical Operations Lead, Manager, US Clinical Operations, Pfizer Worldwide Research and Development

Marsha (Toby) Johnston, RN, BS, CCRA, Clinical Operations Manager – Oncology, US Clinical Operations, CSO – Development Operations, Pfizer Worldwide Research and Development Paul Kelly, M.S., CCRA, Clinical Research Associate, Infinity Pharmaceuticals, Inc. Paula Kovars, RN, BSN, Associate Director, RCO US Site Monitoring Group, Bristol-Myers Squibb Katie McNamara, Clinical Research Associate, Medical Affairs, BD Medical, BD C. Lynn Meyers, CRA Manager, BD Medical, BD

Carol Opalek, Clinical Research Associate, Abbott Vascular Sharon S. Reinhard, M.S., Associate Director, Clinical Quality Control, Endo Pharmaceuticals Sharon R. Sothern, BA, CCRP, Clinical Research Associate, Clinical Trials Area, Westat Linda Tedder, Clinical Research Manager, Clinical Affairs, DePuy Spine, Inc.