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 monitoring
Responsabilidades
• 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 xqbhyrx 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 environments
Requisitos principales
• insurance plans
• retirement plans
• wellbeing resources
• global recognition programs
• versátil and hybrid working options
• minimum 14 weeks paid parental leave

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