Susy is a clinical research professional with 15 years of varied experience in pharmaceutical and clinical research organisations across data management, clinical operations, project management and quality management; and a deep knowledge of operational issues and challenges within the drug development process.

Susy began her career as a contract Data Manager after graduating, and has progressed through a variety of roles within data management ; also worked as a Clinical Research Associate, and then as a Project Manager. More recently she led a world-wide team responsible processes, training and quality management for a large CRO. During this time she led projects assessing and adopting technology such as Electronic Data Capture, Electronic Document Management and Clinical Trial Management systems. Susy has 5 years experience as a trainer within this role and others and has designed developed and delivered varied training programs to study teams and physicians.

Susy has a passion for process analysis and reengineering to improve the productivity and efficiency of the clinical trial process and in 2008 began work as an independent consultant working with organisations to adopt technology and make the required process and role improvements to maximise the efficiency in their use.

Susy has a BSC Hons from Leeds University and is an active member of the Institute of Clinical Research (ICR), Society for Clinical Data Management (SCDM) and Association for Clinical Data Management (ACDM).