Novo Nordisk has announced an exciting opportunity for Associate Clinical Data Programmer professionals to join its Data Standards and Integration (DSI) team in Bangalore, Karnataka. Candidates with experience in Clinical Data Programming, EDC build, CDISC standards, SQL, Python, SAS, or Veeva EDC can apply for this role.
This position offers the opportunity to work on global clinical trials, build clinical databases, develop API-based data pipelines, and contribute to the delivery of life-changing therapies through high-quality clinical data management.
Job Overview
| Particular | Details |
|---|---|
| Company | Novo Nordisk |
| Job Title | Associate Clinical Data Programmer |
| Department | Data Standards and Integration (DSI) |
| Category | Data & AI |
| Location | Bangalore, Karnataka |
| Job Type | Full-Time |
| Last Date to Apply | 10 August 2026 |
About the Role
The Associate Clinical Data Programmer will support clinical development by designing and maintaining clinical study databases, integrating data from multiple external sources, and ensuring standardized, high-quality clinical datasets for regulatory submissions.
The role involves working closely with Clinical Data Management, Biostatistics, Clinical Operations, AI & Digital Innovation teams, and external CROs to deliver robust data solutions.
Key Responsibilities
- Design and build clinical study databases (EDC/CDMS).
- Configure clinical databases for SDTM data generation.
- Develop API-based clinical data ingestion pipelines.
- Acquire, transform and harmonize clinical trial data.
- Maintain standardized clinical data flows.
- Perform User Acceptance Testing (UAT).
- Monitor daily clinical data loads.
- Troubleshoot data integration issues.
- Support Managed File Transfer (MFT) processes.
- Collaborate with internal stakeholders and external vendors.
- Follow CDISC, CDASH and SDTM standards.
- Promote best practices across clinical programming projects.
Who Can Apply?
Candidates possessing any of the following qualifications may apply:
- B.Sc Life Sciences
- M.Sc Life Sciences
- B.Sc Computer Science
- M.Sc Computer Science
- Information Technology
- Clinical Information Management
- Equivalent relevant qualification
Required Experience
- 2โ4 years in the pharmaceutical or clinical research industry.
- Minimum 2 years of end-to-end clinical database setup experience.
- Experience with Veeva EDC/CDB preferred.
- Experience with clinical database programming.
Required Skills
Applicants should have knowledge of:
- Clinical Data Programming
- Clinical Data Management
- EDC Build
- CDMS
- Veeva EDC
- Oracle InForm
- CDISC
- CDASH
- SDTM
- SQL
- Python
- SAS
- R Programming
- Azure Databricks
- API Integration
- User Acceptance Testing (UAT)
- Clinical Data Integration
- Medical Terminology
- GxP Compliance
- AI & Machine Learning basics
Salary (Estimated)
Based on similar Clinical Data Programming roles in Bengaluru, the expected salary may range between:
โน8,00,000 โ โน15,00,000 per annum (CTC)
Actual compensation depends on experience, technical skills, and internal compensation policies.
Why Join Novo Nordisk?
Employees can expect:
- Global pharmaceutical career exposure
- Opportunities to work on innovative clinical trials
- Learning and development programs
- Modern AI-enabled clinical data platforms
- Collaborative global teams
- Inclusive work culture
- Career growth within Research & Development
- Competitive salary and employee benefits
How to Apply
