Remoto: Trabajo híbrido

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.insurance plansglobal recognition programsflexible and hybrid working optionsminimum 14 weeks paid parental leaveContribute to Central Monitoring Platform outputs development using SAS programming and clinical data standardsDevelop analytics dashboards, reports (KRIs, QTLs, DQA) and data pipelines for clinical operationsTranslate business needs into scalable technical solutions to improve user experiencePerform ETL: extract, clean, merge, subset, and derive clinical and operational datasetsPartner with study teams, statisticians, and Central Monitoring colleagues to clarify output requirementsParticipate in quality checks and validation routines to ensure complete,



accurate reports and monitoring dataSupport existing dashboards, reports, and pipelines through scheduled refreshes and performance monitoringBachelor’s degree in Life Sciences, Computer Science, Data Science, Engineering, Statistics, or related field2-3 years of experience in clinical programming, clinical data analytics, or Risk-Based Quality ManagementKnowledge of SAS/R programming and SAS data handling tasksWorking knowledge of SAS, AI/ML, R/Python/SQL; ability to write clean code and queriesFamiliarity with BI tools (Power BI, Spotfire, Tableau) for visualizationsStrong understanding of clinical trial data structures and processesExperience developing Key Risk Indicators, Quality Tolerance Limits, analytics outputs, or monitoring reportsKnowledge of Risk-Based Quality Management principles and cross-functional collaboration in clinical development environmentsCross-functional collaborationAnalytical mindsetProblem-solvingSAS programmingR/Python/SQLBI tools (Power BI, Spotfire, Tableau)Associate Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring - Novartis • barcelona, catalunya, es#J-18808-Ljbffr

📌 Associate Clinical Programmer - Clinical Study Data, Risk Based Quality Management & Monitoring - No (Madrid)
🏢 Novartis
📍 Madrid