Clinical Data Management Jobs at Novo Nordisk
A rare chance has emerged for aspiring professionals in clinical data management jobs at Novo Nordisk. The company is seeking an Associate Clinical Data Programmer in Bangalore, Karnataka, to contribute to the development of life-changing therapies. This role offers an exciting opportunity to shape how clinical data flows from trials to treatment.
About Novo Nordisk
Novo Nordisk is a global healthcare company focused on innovative solutions to chronic diseases. Headquartered in Denmark, the organization operates in the pharmaceutical sector, specializing in diabetes care, obesity treatment, and hormone replacement therapy. With a commitment to sustainability and a patient-centered approach, Novo Nordisk aims to improve the lives of millions worldwide. The company is currently offering clinical data management jobs, including the position of Associate Clinical Data Programmer, to enhance its capabilities in clinical research.
Job Details
- Job Title: Associate Clinical Data Programmer
- Company: Global Business Services, India
- Department: Data Standards and Integration
- Location: Bangalore, Karnataka, IN
- Deadline: 10 August 2026
Job Description
As an Associate Clinical Data Programmer in Data Standards & Integration (DSI) at Novo Nordisk, the successful candidate will play a pivotal role in designing, building, and maintaining clinical study databases and data pipelines that are crucial for clinical trials. This position directly supports the generation of high-quality data necessary for regulatory submissions, ultimately ensuring that vital medicines reach patients in need.
Key Responsibilities
- 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 the NextGen data platform.
- Acquiring, transforming, harmonizing, and integrating raw clinical data from multiple external sources to ensure seamless data availability for downstream consumers.
- Performing configurations and transformational updates within the next-generation framework to establish standardized 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 organization and ensuring learnings are implemented in forthcoming trials and projects.
Eligibility Criteria
- A minimum M.Sc or B.Sc in Life Science, Clinical Information Management, or equivalent qualification.
- 2–4 years of experience in the pharmaceutical industry, including at least 2 years of hands-on end-to-end clinical database set-up activities (preferably Veeva EDC/CDB) with working knowledge of CDASH, SDTM, and CDISC standards.
- Fluency in programming languages such as SQL, CQL, R, Python, Azure Databricks, or SAS, and experience designing and implementing API integrations for clinical data acquisition.
- Strong understanding of protocol design, CRF standards, InForm/Veeva terminologies, EDC data structures, GxP practices, and medical terminology.
- Basic knowledge of AI & ML concepts to contribute to automation initiatives.
- A proactive, solution-oriented mindset with strong analytical skills, the ability to prioritize competing demands, and fluency in written and spoken English.
Why Join Novo Nordisk?
At Novo Nordisk, employees are driven by a shared purpose to improve the lives of people living with chronic diseases. The company fosters a culture of determination, curiosity, and mutual respect, which leads to extraordinary results. Working at Novo Nordisk not only provides the chance to contribute to meaningful healthcare solutions but also offers numerous opportunities for professional development and personal growth. The organization values diverse thinking and encourages innovative ideas, making it an ideal place for those pursuing clinical data programmer jobs in India.
Conclusion
This is a remarkable opportunity for candidates interested in clinical data management jobs at Novo Nordisk. The role of Associate Clinical Data Programmer in Bangalore not only promises professional growth but also the chance to make a significant impact on patient care. Interested individuals are encouraged to apply before the deadline of 10 August 2026 to become part of Novo Nordisk’s mission to deliver innovative healthcare solutions.
