ph3Summary /h3 pLocation: Barcelona Gran Via /p pRelocation Support: Relocation support is typically not available for this role; /p pPlease 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. /p pImagine 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. /p h3About The Role /h3 h3Key Responsibilities /h3 ul liContribute to Central Monitoring Platform outputs development using Statistical Analysis System programming and clinical data standards. /li liDevelop analytics dashboards, reports ( KRIs, QTLs and DQA like statistical tests), data pipelines, and monitoring outputs for clinical operations. /li liTranslate business needs into practical, scalable technical solutions that improve user experience. /li liPerform operations like Extract, clean, merge, subset, and derive clinical and operational datasets. /li liPartner with study teams, statisticians, and Central Monitoring colleagues to clarify output requirements. /li liParticipate in quality checks and validation routines to ensure complete, accurate reports monitoring data. /li liSupport existing dashboards, reports, and pipelines through scheduled refreshes and performance monitoring. /li /ul h3Essential Requirements /h3 ul liBachelor’s degree in Life Sciences, Computer Science, Data Science,



Engineering, Statistics, or a related field. /li liIdeally 2-3 years of experience in clinical programming, clinical data analytics, or Risk-Based Quality Management. Knowledge and capabilities in SAS/R programming. /li liStatistical Analysis System programming exposure, including tasks such as data extraction, transformation, derivation, and reporting. /li liWorking knowledge of SAS, AI/ML, R/Python/SQL; ability to write clean, simple code and queries. /li liFamiliarity with BI tools (Power BI, Spotfire, Tableau) for standard visualizations. /li liStrong understanding of clinical trial data structures and clinical operations processes. /li liExperience developing Key Risk Indicators, Quality Tolerance Limits, analytics outputs, or monitoring reports. /li liWorking knowledge of Risk-Based Quality Management principles and cross-functional collaboration within clinical development environments. /li /ul h3Desirable Requirements /h3 ul liExperience working in a clinical operations environment with Risk-Based Quality Management and knowledge of CluePoints platform /li liUnderstanding of Clinical Data Interchange Standards Consortium standards, including Study Data Tabulation Model (SDTM and Analysis Data Model (ADaM). /li /ul h3Benefits Rewards /h3 pAt Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. /p pThe expected Annual Base Salary Range for this role: €27,900.00 - 51,900.00 /p pThe base salary offered is determined based on gender-neutral objectives, such as relevant skills,



competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. /p pIn addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. /p ul liinsurance plans /li liretirement plans /li liwellbeing resources /li liglobal recognition programs /li liflexible and hybrid working options /li liminimum 14 weeks paid parental leave /li /ul pPay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. /p pRead our brochure to learn more about our integral total rewards offering: /p pNote: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. /p h3Commitment to Diversity and Inclusion / EEO /h3 pNovartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve. /p h3Why Novartis: /h3 pHelping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? /p h3Benefits Rewards: /h3 pLearn about all the ways we’ll help you thrive personally and professionally. /p pRead our handbook (PDF 30 MB) /p /p #J-18808-Ljbffr

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