ph3Summary /h3pLocation: Barcelona Gran Via /ppRelocation Support: Relocation support is typically not available for this role; however, it can be discussed if selected for an interview. /ppImagine 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. /ph3About The Role /h3h3Key Responsibilities /h3ulliConfigure Central Monitoring Platform outputs using SAS programming and clinical data standards /liliDevelop analytics dashboards, reports, data pipelines, and monitoring outputs for clinical operations /liliTranslate business needs into practical, scalable technical solutions that improve user experience /liliExtract, clean, merge, subset, and derive clinical and operational datasets /liliPartner with study teams, statisticians, and Central Monitoring colleagues to clarify output requirements /liliExecute quality checks and validation routines to ensure complete, accurate monitoring data /liliSupport existing dashboards, reports, and pipelines through scheduled refreshes and performance monitoring /liliCoach associate programmers, share technical knowledge, and contribute to reusable programming standards /li /ulh3Essential Requirements /h3ulliBachelor’s degree in Life Sciences, Computer Science, Data Science, Engineering, Statistics, or a related field /liliIdeally 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 /liliAdvanced Clinical programming expertise, including data extraction, transformation, derivation, and reporting /liliClinical data analytics, reporting, RbQM, or technology implementation proven track on complex integrations and BI at scale /liliWorking knowledge of SAS, AI/ML, R/Python/SQL; ability to write clean, simple code and queries /liliFamiliarity with BI tools (Power BI, Spotfire, Tableau) for standard visualizations /liliStrong understanding of clinical trial data structures and clinical operations processes /liliUse of AI tools for processes, automation and real-time data analytics /liliExperience developing Key Risk Indicators, Quality Tolerance Limits, analytics outputs, or monitoring reports /liliWorking knowledge of Risk-Based Quality Management principles and cross-functional collaboration within clinical development environments /li /ulh3Desirable Requirements /h3ulliExperience working with CluePoints monitoring platform /liliUnderstanding of Clinical Data Interchange Standards Consortium standards, including Study Data Tabulation Model (SDTM and Analysis Data Model (ADaM)) /li /ulh3Benefits Rewards /h3pAt Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. /ppExpected Annual Base Salary Range for role: € 36,100.00 - 67,100.00 /ppThe 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.



/ppIn addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. /ppThe rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave. /ppPay 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. /ppRead our brochure to learn more about our integral total rewards offering: /ppNote: 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. /ph3Commitment to Diversity and Inclusion / EEO /h3pNovartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve. /ph3Why Novartis: /h3pHelping 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? /ph3Benefits and Rewards: /h3pLearn about all the ways we’ll help you thrive personally and professionally. /ppRead our handbook (PDF 30 MB) /p /p #J-18808-Ljbffr

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