(HP660) | CTA PAYMENTS

Overviewas a cta, you will join the world's largest and most comprehensive clinical research organization, powered by healthcare intelligence. you will partner with one of the world's leading biopharmaceutical companies. working across a broad portfolio of medicines and vaccines, this company has a long-standing heritage of delivering innovative treatments and preventive medicines globally. responsibilitieswhat you will be doing: the cta assists in coordinating and administering study activities from startup to execution and closeout, ensuring quality and consistency of interventional study deliverables within the local study team, meeting time, cost, and quality objectives. collects, prepares, reviews, and tracks documents for the application process, and coordinates study materials and equipment.assists in submitting proper applications/documents to ec/irb and regulatory authorities where appropriate.interfaces with investigators, external service providers, and cras during document collection.acts as the local administrative main contact, working closely with cras and lsad throughout the study.sets up and maintains the local etmf and isf, including document tracking per ich-gcp and local requirements.ensures timely upload of essential documents to maintain etmf inspection readiness and supports cra in study close-out activities.prepares or supports site contract preparation, where applicable.leads practical arrangements for meetings, handles document printing/distribution, and archives study-related emails.collaborates with data management centre and global clinical ...