Get a Free Listing!
All Categories

Clinical Training Forum

Date: 11-Oct-12 to 12-Oct-12
Location: Le Meridien / Cambridge / Massachusetts / United States
Category: Healthcare & Pharmaceuticals Science Conferences & Trade Fairs

Overcome training challenges with the leading industry approaches and best practices offered at Barnett International and Cambridge Healthtech Institute’s fourth annual Clinical Training Forum. 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, Clinical Project Management and Virtual Investigator Meeting Management.

Visitors

This summit particularly benefits professionals at pharmaceutical,
biotech and medical device companies who work in:
• Clinical Trial Management
• Site Management
• Study Start-up
• Project Management
• Monitoring
• Clinical Training
• Medical Writing
• Protocol Development
• GCP Compliance
• Clinical Operations
• Budgeting
• CRA Management
• Study Site Evaluations
• Risk Management
• Outsourcing

The summit is also of interest to:
• Contract Research Organizations
• Regulatory Agencies
• Technology and Service Vendors
• Consultants

Exhibitors

Learn more about our sponsors at http://www.barnettclinicalsummit.com/bcs_content.aspx?id=105595&libID=105552

Go to event website