CTA

As a CTA, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. CTA assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives. Responsibilities include document collection, assisting in the application process to EC/IRB and Regulatory Authorities, interfacing with Investigators, external service providers and CRAs, and setting up and maintaining the local eTMF and ISF. The role also involves preparing contracts at a site level, coordinating internal and external meetings, and ensuring compliance with local legislation.