Shape how clinical data flows from trial to treatment – and help bring life-changing therapies to patients faster.
Your current 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 new 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, and human data to dev
📌 Associate Clinical Data Programmer (Bengaluru)
🏢 Novo Nordisk
📍 Bengaluru
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