Exciting pharma jobs opportunity for experienced professionals! Novo Nordisk is hiring a Senior Clinical Data Scientist in Bangalore. This is a great chance for candidates seeking pharmaceutical careers in India with a global leader in diabetes and chronic disease research.
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About the Company
Novo Nordisk is a world-renowned Danish pharmaceutical company with over 100 years of excellence in defeating serious chronic diseases.
Known for innovation, regulatory compliance, and cutting-edge Research & Development, the company operates globally with a strong presence in India through its Global Business Services (GBS) center in Bangalore. It combines advanced AI tools, human data, and scientific curiosity to deliver life-changing therapies while maintaining the highest standards of quality and patient safety.
Job Details
- Company Name: Novo Nordisk
- Experience: 3-5 years of statistical programming experience (preferably 1 year in pharmaceutical industry)
- Qualification: Bachelor’s or Master’s degree in Life Sciences, Natural Sciences, Engineering, or equivalent
- Location: Bangalore, Karnataka, India
- Work Type: On-site
Job Description
Novo Nordisk is looking for a talented Senior Clinical Data Scientist to join its Clinical Data Science team in Bangalore. This role plays a critical operational role within trial squads, bridging complex data programming with clinical development to support groundbreaking therapies for chronic diseases.
Position Title: Senior Clinical Data Scientist
- Department: Bangalore R&D – Clinical Data Science
- Market: Global Business Services (GBS) India
- Role: Operational partner in clinical trials focusing on data science, statistical programming, and regulatory submissions
- Experience: 3-5 years
- Education/Qualification: Bachelor’s/Master’s in Life Sciences, Natural Sciences, Engineering or equivalent
Skills/Qualifications
- Strong expertise in SAS or R programming for clinical trial reporting, analysis, and data handling
- Solid understanding of SDTM and ADaM standards, eCRF design, Data Flow Plans, and Blinding Plans
- Knowledge of drug development processes, clinical database technologies, and GxP guidelines
- Experience in program review, documentation, and submission package preparation
- Excellent planning, coordination, and stakeholder management skills
- Outstanding written and spoken English communication with cross-cultural collaboration experience
- Self-driven, analytical thinker with problem-solving mindset and ability to manage multiple priorities
Key Responsibilities
- Lead clinical data science setup for trials including eCRF and blinding plans
- Ensure quality of SDTM/ADaM deliverables and TFL generation
- Review protocols and Statistical Analysis Plans
- Coordinate with CROs and vendors for smooth trial execution
- Contribute to regulatory documents like Risk Management Plans and Investigator’s Brochures
- Facilitate knowledge sharing sessions post-submission
- Drive process improvements and present at global forums
Benefits/Perks
- Opportunity to work on innovative global clinical projects
- Strong focus on continuous learning and professional development
- Exposure to international standards and cross-functional collaboration
- Inclusive work culture with emphasis on diversity and mutual respect
- Long-term career growth in a purpose-driven organization
- Competitive compensation and benefits package
How to Apply
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Novo Nordisk career page.

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Interested candidates can apply directly through the Novo Nordisk career portal. Upload your updated CV and follow the application instructions on their official website.
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Deadline: Applications are invited on a rolling basis. Apply promptly.
Why You Should Join
Joining Novo Nordisk means becoming part of a legacy that has improved millions of lives worldwide. The company offers exceptional pharmaceutical careers in India with a perfect blend of scientific innovation, operational excellence, and long-term stability. You’ll work in a collaborative environment that values fresh ideas, continuous learning, and meaningful impact on global healthcare.
FAQs
Q1. What is the experience required for Senior Clinical Data Scientist at Novo Nordisk?
A: Candidates need 3-5 years of statistical programming experience, preferably with 1 year in the pharmaceutical industry.
Q2. Is this position based in Bangalore only?
A: Yes, the role is located at Novo Nordisk Global Business Services in Bangalore, Karnataka.
Q3. What programming languages are mandatory?
A: Extensive knowledge of SAS or R is required for clinical trial data analysis and reporting.
Q4. How can I apply for this pharma job?
A: Submit your application online via the Novo Nordisk career page with your latest CV.