I am a highly motivated, flexible and committed individual with exceptional communication skills and twenty five years’ experience in Clinical Operations, Outsourcing and Learning within Pharmaceutical Research and Development.Extensive Clinical Development and Operations experience in all pre-registration trial phases including clinical pharmacology studies. Wide ranging therapeutic area knowledge gained in Contract Research Organisations (CRO), large pharmaceutical and small biotechnology companies. Currently Global Clinical Program Excellence Lead within a major pharmaceutical company and responsible for several study management processes, including Risk Based Quality Management. Providing far ranging process consultancy and subject matter expertise on major infrastructure projects including implementation of a new Clinical Trial Management System and Clinical Data Management Suite as well as continuous process and system improvement projects. Previously provided learning consultancy and learning event development expertise within the same company.Responsible in prior roles for overall delivery of early development programs in a small biotechnology company, including complex, multipart and flexible protocols, with significant contributions made to study design and protocol development. Accountable for outsourcing clinical development activities, including entire functions and for development of standardized tools and processes. Major contributor in the development and implementation of a Quality Management system, including full responsibility for preparing clinical development Standard Operating Procedures (SOPs).I have a Bachelor of Science degree in Physiology and Pharmacology from University of Southampton, UK and Post Graduate Diploma in General Management from Macquarie Graduate School of Management, NSW Australia.