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# Expert Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring

- **Company:** Novartis
- **Location:** Barcelona, Spain
- **Salary:** €36,100.0 - €67,100.0
- **Contract:** Permanent contract
- **Skills:** Artificial Intelligence, Data Analysis, Clinical Data Management, Clinical Data Repository, Data Mining, R (Programming Language), Python (Programming Language), Power BI, SAS (Software), SQL Databases, Systems Integration, Tableau (Software), Information Technology, Data Analytics, Performance Monitor, Real Time Data, Spotfire, Data Pipelines
- **Published:** July 23, 2026
- **Apply:** https://es.indeed.com/viewjob?jk=4e4d123a322b8a59

## About the Role

* Bachelor's degree in Life Sciences, Computer Science, Data Science, Engineering, Statistics, or a related field

 * Ideally 6-7 years of experience in clinical programming, clinical data analytics, with good knowledge in Risk-Based Quality Management. Expertise in RBQM KRI, QTL programming and analysis, SAS/R programming, project management exposure and knowledge of CluePoints like central monitoring platform is preferred

 * Advanced Clinical programming expertise, including data extraction, transformation, derivation, and reporting

 * Clinical data analytics, reporting, RbQM, or technology implementation proven track on complex integrations and BI at scale

 * Working knowledge of SAS, AI/ML, R/Python/SQL; ability to write clean, simple code and queries

 * Familiarity with BI tools (Power BI, Spotfire, Tableau) for standard visualizations

 * Strong understanding of clinical trial data structures and clinical operations processes
 * Use of AI tools for processes, automation and real-time data analytics

 * Experience developing Key Risk Indicators, Quality Tolerance Limits, analytics outputs, or monitoring reports

 * Working knowledge of Risk-Based Quality Management principles and cross-functional collaboration within clinical development environments

Desirable Requirements

 * Experience working with CluePoints monitoring platform

 * Understanding of Clinical Data Interchange Standards Consortium standards, including Study Data Tabulation Model (SDTM and Analysis Data Model (ADaM)

## Description

Imagine transforming complex clinical trial data into actionable insights that accelerate medical innovation and improve patient outcomes worldwide. As a Clinical Programmer - Expert at Novartis, you will play a pivotal role in advancing Risk-Based Quality Management (RbQM) and our Central Monitoring platform. You will be responsible for 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., * Configure Central Monitoring Platform outputs using SAS programming and clinical data standards

 * Develop analytics dashboards, reports, data pipelines, and monitoring outputs for clinical operations

 * Translate business needs into practical, scalable technical solutions that improve user experience

 * Extract, clean, merge, subset, and derive clinical and operational datasets

 * Partner with study teams, statisticians, and Central Monitoring colleagues to clarify output requirements

 * Execute quality checks and validation routines to ensure complete, accurate monitoring data

 * Support existing dashboards, reports, and pipelines through scheduled refreshes and performance monitoring

 * Coach associate programmers, share technical knowledge, and contribute to reusable programming standards


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