Russell Brierley Joins Y-PRIME as Product Director, IRT & CSM
Brierley is an industry expert with 30 years of experience in clinical supply chain management and drug development and he has served in leadership positions across the spectrum of distribution, packaging, manufacturing and process development/improvement. At Y-Prime Brierley is responsible for continuing the strong growth of the company's IRT solution and driving market acceptance of the newly introduced eCSF, a Clinical Trial Supply & Forecasting platform – two intuitive and powerful tools that optimize decision-making and productivity as well as cost.
"We continue to invest in bright, forward-thinking innovators who have the clinical research skills and experience needed to help our clients plan and manage clinical trials," said
Prior to joining Y-Prime, Brierley served as Senior Director of North American Clinical Supply Chain, Senior Director of Clinical Development Manufacturing and Director of
"Y-Prime's eClinical Solutions are best-in-class technologies that can help sponsors and clinical research organizations achieve a high degree of efficiency," said Brierley. "I look forward to growing our customer base and to further integrating and advancing our IRT and CSM technologies to meet the needs of our clients in an increasingly competitive and complex clinical and regulatory environment."
IRT & eCSF
Y-Prime's Interactive Response Technology (IRT) is a cloud-based eClinical platform that solves challenges with patient randomization and clinical supplies management while providing real-time reporting via web and/or telephone user interfaces (IWR and IVR) that are natively integrated with all major Lab, EDC, CTMS and Depot platforms. It is a fluid, fully customizable system that can be rapidly configured to reduce waste and ensure accurate delivery of product while meeting study timelines.
Y-Prime recently introduced eCSF, a Clinical Trial Supply & Forecasting solution that enhances the ability to minimize drug overages, provides a high degree of visibility at the global, depot or individual site level, and allows sponsors to forecast and manage drug supply for clinical trials in real time.
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Read the full story at http://www.prweb.com/releases/2014/06/prweb11940770.htm
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