Associate Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring
Novartis
Barcelona Gran Vía, ESPosted Discovered via the company's careers siteMatch locked
HybridFULL TIME
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About the role
#LI-HybridLocation: Barcelona Gran ViaRelocation 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.
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Who can apply
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