Shape how clinical data flows from trial to treatment – and help bring life-changing therapies to patients faster.
Your new role
As an Associate Clinical Data Programmer in Data Standards & Integration (DSI), you will play a central role in designing, building and maintaining clinical study databases and data pipelines that power our clinical trials. Your work will directly enable the generation of high-quality data that supports regulatory submissions and gets medicines to patients who need them.
Day-to-day Your Tasks Will Include
• Designing and setting up study databases (EDC and CDMS build) leading up to SDTM data generation for clinical trials of medium to high complexity
• Developing, configuring and maintaining API-based data ingestion pipelines to securely acquire data from external vendors and third-party systems into our NextGen data platform
• Acquiring, transforming,
harmonising and integrating raw clinical data from multiple external sources to ensure seamless data availability for downstream consumers
• Performing configurations and transformational updates within our next-generation framework to establish standardised data flows and a single source of truth
• Executing and documenting User Acceptance Testing to ensure databases meet specification requirements before deployment into production
• Monitoring daily data loads across relevant systems, troubleshooting error incidents and supporting internal stakeholders and vendors through the Managed File Transfer process
• Promoting the exchange of best practices within the organisation and ensuring learnings are implemented in forthcoming trials and projects
Your current department
In Research & Development, you'll be part of a unit that explores bold scientific ideas and advances them into clinical testing. We combine curiosity, AI tools, an
📌 Associate Clinical Data Programmer (Bengaluru)
🏢 Novo Nordisk
📍 Bengaluru
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