Clinical Trial Associate

As a CTA, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. As a Clinical Trial Assistant, you'll have a fundamental role in the successful execution of global clinical trials. Key responsibilities involve supporting the completion and coordination of various logistical and administrative tasks within the Clinical Development Plan and ICH-GCP guidelines. Your duties will include supporting the study team, collecting data for regulatory submissions, document tracking (contracts, financial agreements, patient informed consent forms, insurance certificates) and managing the delivery of non-drug related study supplies. Maintain constructive relationships with site staff and tracking site budget related matters. You may also be responsible for scheduling meetings, updating Excel trackers, coordinating document translation and providing ad-hoc support.