Electronic Data Capture for Clinical Trials

This FREE webinar was recorded on:
Thursday, April 04, 2013
10:00 AM - 11:00 AM EDT
Electronic Data Capture for Clinical Trials

How do we ensure our clinical research increases in effectiveness and efficiency while decreasing costs?
Many have tried to solve this question by outsourcing to Contract Research Organisations (CROs) who have to look closely into their own business to ensure they can maintain their value. In order to do this they often ask for just one technology platform that will work for the entire clinical process, rather than just point solutions. This increases efficiency through a series of individual process improvements as well as improved decisions through metrics and analytics.


Nicholas Kenny, PhD
Executive Vice President and General Manager, Global Oncology and Hematology
INC Research

Dr. Kenny has 25 years of research and development experience. Dr. Kenny’s industry career began as a Clinical Research Fellow. He moved into management roles within the CRO industry, where he was responsible for establishing the strategic direction of clinical programs, as well as having global oversight of project management, clinical monitoring, and regulatory staff. He has provided clinical development and regulatory strategy consulting services, international project management, and process development and integration expertise to a variety of pharmaceutical and biotech companies. Over the past 10 years Dr. Kenny’s drug development expertise has been primarily focused upon oncology clinical development.

Prior to his move to industry, Dr. Kenny spent 15 years in endocrinology and cell biology research and teaching in the United Kingdom, Canada, and the United States (US) where he was Assistant Professor in the College of Medicine at the University of Vermont. He was also a National Institute of Health Research Fellow at McGill University and received his PhD in Reproductive Endocrinology from the University of Hull, United Kingdom.

Joe Dustin
Senior Pre-Sales Business Consultant
Medidata Solutions

Joe Dustin has over 10 years experience in Healthcare Technology and eClinical Trials, including positions in Consulting, Project Management and IT. Currently, as a Sr. Business Consultant with Medidata Solutions, Joe is responsible for mapping out solutions to conduct and optimize Clinical Trials in the cloud using a mix of state of the art technology, process and design. Joe works with some of the largest Pharmaceutical, Biotech, Academic, Government and Contract Research Organizations (CROs) in the world regarding technology adoption, change management and interoperability.