Summary

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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 general clinical studies.

About The Role
Key Responsibilities

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- 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 derive clinical and operational datasets.
- Partner with study teams, statisticians, and Central Monitoring colleagues to clarify output requirements.
- Participate in quality checks and validation routines to ensure complete, accurate reports monitoring data.
- Support existing dashboards, reports, and pipelines through scheduled refreshes and performance monitoring.

Essential Requirements

📌 Associate Clinical Programmer (Barcelona)
🏢 Novartis
📍 Barcelona