Applying Unified E-clinical Technologies to Streamline Study Conduct
Sponsors and CROs use an average of six applications to support clinical trial activities, 52% of CROs report that they still use paper forms to support their studies, and an average of $1M/day is lost for everyday the trial runs late.
In this webinar, Medidata will conduct an interactive demo of our intelligent platform for life sciences—exploring our broader EDC, RTSM and ePRO capabilities—and show how adopting one platform can help unify your data and workflows across study execution, allowing for rapid study startup, more streamlined execution with cleaner data, and the elimination of unnecessary reconciliation efforts.
Date: Wednesday, December 12, 2018
Time: 1PM EST
VP of Product, Study Conduct Solutions
Wayne is Vice President of Product Management for Rave, Coder, Rave Safety Gateway, and Platform that includes Cloud Administration and iMedidata. He joined Medidata in January, 2017 and has also had stints of product responsibilities for Imaging, RCM/eTMF, and RTSM. Prior to joining Medidata, Wayne spent 12 years overseeing Product Management for clinical technology used by Data Management and Biometrics at PRA Health Sciences. This involved oversight of Platform as a Service, Software as a Service, on premise deployed environments, and in-house developed solutions.
Sr. Director, Product -- RAVE RTSM
As the Senior Director of Product for Rave RTSM, Kevin is focused on development and delivery of Medidata's Randomization and Trial Supply Management (RTSM) solution - Rave RTSM. Kevin has spent his entire 28+ year career in the Life Sciences arena working in clinical research, medical devices, systems and software delivery and project management. He has a well-rounded background that is technology focused and includes a deep understanding of the clinical trial life-cycle and the Pharmaceutical industry. Kevin honed his IRT/RTSM skills at Icon where he led the Project Management team responsible for large clients and was instrumental in unique and innovative IRT design initiatives. Immediately prior to joining Medidata, Kevin provided consulting in the Pharmaceutical R&D space at Accenture where he primarily focused on e-clinical technology, R&D IT strategy, data analytics, and solution assessments. His past experience in software development and system delivery gives him invaluable insight to what Medidata's customers are concerned with in their IT and Clinical Operations departments.
Solution Consultant II
Greg joined Medidata in 2014 and has been focused on product adoption and understanding client needs during that time. Prior to Medidata, Greg spent 7 years with PPD focused on EDC usage/support and in Data Management. Greg also held roles within Pfizer and other small pharma organizations, again focused on EDC usage and support.