Associate Clinical Data Programmer (Bangalore, Karnataka, IN)

Biopharma Careers; Bengaluru; On-site; INR 900,000 - 1,200,000; Full time

Job summary

Novo Nordisk Bangalore seeks an Associate Clinical Data Programmer to design, build and maintain clinical study databases and data pipelines powering trials. You will enable high‑quality data for regulatory submissions and faster patient access.

You will work within Data Standards & Integration, collaborating with Clinical Data Management, Biostatistics, and external vendors to deliver robust data solutions across trials. Strong SQL, Python and Veeva EDC experience is essential.

Qualifications

• M.Sc or B.Sc in Life Science, Computer Science, IT, Clinical Information Management or equivalent qualification.
• 2–4 years of pharma industry experience with end‑to‑end clinical database setup (preferably Veeva EDC/CDB) and knowledge of CDASH, SDTM and CDISC.
• Fluency in SQL, CQL, R, Python, Azure Databricks or SAS; experience with API integrations for clinical data ingestion.
• Strong understanding of protocol design, CRF standards, InForm/Veeva terminologies, EDC data structures, GxP and medical terminology.
• Basic knowledge of AI & ML concepts for automation initiatives.
• Proactive, solution‑oriented mindset with strong analytical skills; fluent in written and spoken English.

Responsibilities

• Design and set up study databases (EDC and CDMS) and generate SDTM data for medium to high complexity trials.
• Develop, configure and maintain API‑based data ingestion pipelines from external vendors into the NextGen data platform.
• Acquire, transform and harmonise raw clinical data from multiple sources for downstream use.
• Configure and update data flows in the next‑gen framework to standardise processes.
• Perform and document User Acceptance Testing before production deployment.
• Monitor daily data loads and troubleshoot errors with stakeholders and vendors.

Skills

SQL

CQL

R

Python

Azure Databricks

SAS

API integrations

English fluency

Education

M.Sc or B.Sc in Life Science, Computer Science, IT, Clinical Information Management or equivalent

Tools

Veeva EDC

CDMS

Job description

Job Title – Associate Clinical Data Programmer

Company – Novo Nordisk Global Business Services (GBS)

Department – Data Standards and Integration

Location – Bangalore

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 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 develop transformative therapies. Through collaboration and operational excellence, we shape and deliver an innovative pipeline to meet future patient needs.

Within R&D, you will join Data Standards & Integration (DSI) in Global Development, Bangalore. The team is responsible for end‑to‑end clinical data programming – from database design and set‑up through to data ingestion and standardisation – across our growing trial portfolio. You will collaborate closely with Clinical Data Management, Biostatistics, Clinical Operations, AI & Digital Innovation and external vendors/CROs to deliver robust data solutions that accelerate our pipeline.

Your skills & qualifications

We’re looking for an Associate Clinical Data Programmer who thrives in a technically demanding environment and is energised by solving complex data challenges. You’ll bring with you:

• A minimum M.Sc or B.Sc in Life Science, Computer Science, Information Technology, 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 prioritise competing demands, and fluency in written and spoken English

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long‑term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you’re not just starting a job – you’re becoming part of a story that spans generations.

What we offer

There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.

Deadline

4th Sep 2026

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

About Novo Nordisk

At Novo Nordisk, we’re not chasing quick fixes – we’re creating lasting change for long‑term health. For over 100 years, we’ve been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what’s possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we’re making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.