Experteer Overview La siguiente información tiene como objetivo proporcionar a los posibles candidatos una mejor comprensión de los requisitos para este puesto. In this role you contribute to the Central Monitoring Platform and Risk-Based Quality Management initiatives by turning clinical data into actionable insights. You will work with cross-functional teams to design analytics outputs, dashboards, and data pipelines that support clinical operations and smarter decision-making. The role combines data-driven analytics with scalable tech solutions to improve study quality and patient outcomes. This is a hybrid, Barcelona-based opportunity with a strong emphasis on impact and collaboration.Compensaciones / Beneficios• Contribute to Central Monitoring Platform outputs development using SAS programming and clinical data standards• Develop analytics dashboards, reports (KRIs, QTLs, DQA) and data pipelines for clinical operations• Translate business needs into scalable technical solutions to improve user experience• Perform ETL: 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 and monitoring data• Support existing dashboards, reports, and pipelines through scheduled refreshes and performance monitoringResponsabilidades• Bachelor’s degree in Life Sciences, Computer Science, Data Science, Engineering, Statistics, or related field• 2-3 years of experience in clinical programming, clinical data analytics, or Risk-Based Quality Management• Knowledge of SAS/R programming and SAS data handling tasks• Working knowledge of SAS, AI/ML, R/Python/SQL; ability to write clean code and queries• Familiarity with BI xcskxlj tools (Power BI, Spotfire, Tableau) for visualizations• Strong understanding of clinical trial data structures and processes• Experience developing Key Risk Indicators, Quality Tolerance Limits, analytics outputs, or monitoring reports• Knowledge of Risk-Based Quality Management principles and cross-functional collaboration in clinical development environmentsRequisitos principales• insurance plans• retirement plans• wellbeing resources• global recognition programs• adaptable and hybrid working options• minimum 14 weeks paid parental leave

📌 Associate Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring (Barcelona)
🏢 Novartis
📍 Barcelona