Senior Clinical Data Scientist – Novo Nordisk

A new opening has just gone live at Novo Nordisk Global Business Services (GBS) India, and it’s a strong option for statistical programmers who want to move deeper into clinical development. Based in Bengaluru, Karnataka, this role sits at the center of Novo Nordisk’s global clinical trial delivery engine, translating raw trial data into the submission-ready packages that get life-changing therapies approved.

If you’ve been searching for a clinical statistical programming role that combines hands-on SAS/R work with real influence over trial design and submission strategy, this requisition (Job ID 1430143933) is worth a close look. Below, BRJF breaks down the responsibilities, qualifications, salary outlook, and application steps.

Senior Clinical Data Scientist Bangalore: Role Overview

Novo Nordisk GBS India is recruiting a Senior Clinical Data Scientist to join its Clinical Data Science Bangalore team within the Research & Development (R&D) organization. The team has grown from a small start-up function into one of the largest units inside Global Business Services Bangalore, supporting Novo Nordisk’s clinical development portfolio from early-phase studies through product introduction.

As the Senior Clinical Data Scientist, you will act as the operational partner embedded within trial squads, planning, managing, and executing clinical data science contributions across live clinical trials. The mandate spans eCRF (electronic case report form) design, Data Flow Plans, Blinding Plans, SDTM/ADaM deliverables, and TFL (Tables, Figures, and Listings) generation, all measured against Novo Nordisk’s internal specifications and global regulatory standards.

Quick facts about this posting:

1. Company: Novo Nordisk Global Business Services (GBS) India
2. Location: Bengaluru, Karnataka, India
3. Category: Data & AI
4. Department: Research & Development
5. Job ID / Requisition Number: 1430143933
6. Application Deadline: September 9, 2026
7. Listing Status: Live and accepting applications at the time of publication

Key Responsibilities of the Senior Clinical Data Scientist

1. Leading clinical data science setup for trials, including eCRF design, Data Flow Plans, and Blinding Plans, while serving as the key operational partner within trial squads.
2. Ensuring quality control and compliance of SDTM and ADaM deliverables, and managing submission packages and TFL generation in line with industry standards and Novo Nordisk specifications.
3. Coordinating with R&D stakeholders to facilitate open learning sessions and share clinical data science expertise after each submission.
4. Providing critical input into authority-required documents such as Risk Management Plans, Investigator’s Brochures, and Development Safety Update Reports.
5. Managing day-to-day trial execution, reviewing protocols and Statistical Analysis Plans, and contributing to interpretation and communication of clinical trial results.
6. Overseeing collaboration with CROs (Contract Research Organizations) and vendors, and maintaining inspection-readiness documentation throughout the trial lifecycle.
7. Driving process innovation by identifying better practices and presenting improvements at global knowledge-sharing forums.

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Required Qualifications for This Role

1. A Bachelor’s or Master’s degree in life sciences, natural sciences, engineering, or an equivalent discipline.
2. 3–5 years of statistical programming experience, ideally with at least 1 year specifically within the pharmaceutical industry (or equivalent relevant experience).
3. Strong hands-on programming expertise in SAS or R, with proven experience reporting clinical trials, including statistical data handling, analysis, and reporting.
4. Solid knowledge of drug development processes, clinical database technologies, data models, and advanced programming techniques.
5. Experience with program review and documentation, plus a working understanding of GxP guidelines within drug development.
6. Strong planning and coordination skills, including the ability to manage variable workloads and multiple simultaneous priorities.
7. Excellent written and spoken English communication skills, with experience presenting to diverse, cross-regional audiences.