About this role
Jul 21, 2026 Spain Summary Location: Barcelona Gran Via Relocation Support: Relocation support is typically not available for this role; Please only apply if our Barcelona office location is accessible for you. We operate a hybrid working arrangement with an expectation of 12 days a month in office. Imagine transforming complex clinical trial data into actionable insights that accelerate medical innovation and improve patient outcomes worldwide. As an Associate Clinical Programmer at Novartis, you will be significant contributor in advancing Risk-Based Quality Management (RbQM) and our Central Monitoring platform. You will participate in data-driven clinical operations through advanced analytics, intelligent reporting, and scalable technology solutions. Working alongside cross-functional experts, you will help shape the future of clinical data operations by delivering meaningful insights, driving operational excellence, and enabling smarter decisions across global clinical studies. About the Role Key Responsibilities Contribute to Central Monitoring Platform outputs development using Statistical Analysis System programming and clinical data standards. Develop analytics dashboards, reports ( KRIs, QTLs and DQA like statistical tests), data pipelines, and monitoring outputs for clinical operations. Translate business needs into practical, scalable technical solutions that improve user experience. Perform operations like Extract, clean, merge, subset, and