Beverly Barna

Background

About Beverly Barna

Extensive experience in the field of Medical Device clinical trial management. Expertise in study startup and execution of vision care clinical trials including management of CROs and all operational aspects of trials in accordance with FDA regulations, ICH and GCP guidelines through review and approval of clinical report. Manage clinical trial project timelines. Supervise activities of Study Managers and oversee field monitors activities. Review design and development of protocols, CRFs, and clinical reports. Develop project budgets, resource allocation, and expense analysis. 2013-Present Independent Clinical Consultant 2011-2013 Associate Director, Clinical Trial Operations, Vision Care 2006-2011 Manager, Device Clinical Operations (Dual Role - Vision Care and Surgical) 2003-2011 Clinical Project Manager, Vision Care (Dual Role - Vision Care and Surgical) 1996–2003 Senior Clinical Research Associate (Vision Care, Surgical and Pharmaceuticals) 1990-1996 Manager, Clinical Studies, Vision Care 1975-1990 Past Positions: Supervisor of Clinical Studies, Vision Care; Clinical Research Monitor, Vision Care; International Professional Services Administrator; International Program Coordinator