Assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Global Study Team to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives. Your responsibilities include supporting Global Study Director (GSD) / Global Study Associate Director (GSAD) and Global Study Managers (GSMs) by completing delegated study work, initiating and leading the set-up of the electronic Trial Master File (eTMF).
Job listings
Play a key role in improving the lives of patients by accelerating the development of our customers drugs and devices through innovative solutions. You will be dedicated resource to one of our clients, be embedded in their working environment, systems and processes. Collect, prepare, review, approve, process and track regulatory and site level critical documents required for study site activation.