Sr Clinical Data Scientist

Novo Nordisk
Location
Bangalore, Karnataka, IN
Job Type
Full-time
Posted
September 24, 2026
Views
56

Job Description

Department: Research & Developement

Company - Novo Nordisk Global Business Services (GBS) India

Location: Bengaluru

Transform clinical data into life-changing insights that bring breakthrough therapies to patients worldwide.

Your new role

As a Senior Clinical Data Scientist, you'll be the operational partner within trial squads, responsible for planning, managing and executing clinical data science contributions across clinical trials. You'll bridge the gap between complex data programming and clinical development, ensuring that every statistical analysis meets the highest industry standards and drives our mission to defeat serious chronic diseases.

Your responsibilities will include

  • Leading the 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
  • Ensuring quality control and compliance of SDTM and ADaM deliverables, managing submission packages and TFL generation according to industry standards and Novo Nordisk specifications
  • Coordinating with stakeholders across R&D to facilitate open learning sessions and share clinical data science expertise after each submission
  • Providing critical input to authority-required documents including Risk Management Plans, Investigator's Brochures, and Development Safety Update Reports
  • Managing day-to-day trial execution, reviewing protocols and Statistical Analysis Plans, and contributing to the interpretation and communication of clinical trial results
  • Overseeing effective collaboration with CROs and vendors, ensuring inspection readiness documentation is maintained throughout the trial lifecycle
  • Driving innovation by identifying better practices, creating improvements in methods and collaboration, and presenting at global knowledge-sharing forums

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.

You'll join the Clinical Data Science Bangalore team, which has grown from a small start-up to one of the largest units in Global Business Services, Bangalore, and a key contributor to Novo Nordisk's clinical development portfolio. With decades of experience, our team brings together seasoned programmers and fresh perspectives to ensure high-quality statistical analysis and programming support for all clinical development activities worldwide—from early development phases to product introduction.

Your skills & qualifications

We're looking for an analytical thinker who thrives in a fast-paced, collaborative environment and can handle multiple priorities with precision. You'll bring:

  • Bachelor's or Master's degree in life sciences, natural sciences, engineering, or equivalent qualifications
  • 3-5 years of statistical programming experience, with preferably 1 year within the pharmaceutical industry or equivalent relevant experience
  • Extensive programming expertise in SAS or R, with proven experience in reporting clinical trials, including statistical data handling, analysis and reporting
  • Strong knowledge of drug development, clinical database technologies, data models, and advanced programming techniques
  • Experience with program review and documentation, along with in-depth understanding of GxP and guidelines within drug development
  • Excellent planning and coordination skills, with the ability to manage variable workloads and handle numerous tasks simultaneously while maintaining systematic organization
  • Outstanding communication skills in written and spoken English, with experience presenting to diverse audiences and collaborating across professional and regional borders

Department: Research & Developement

Company - Novo Nordisk Global Business Services (GBS) India

Location: Bengaluru

Transform clinical data into life-changing insights that bring breakthrough therapies to patients worldwide.

Your new role

As a Senior Clinical Data Scientist, you'll be the operational partner within trial squads, responsible for planning, managing and executing clinical data science contributions across clinical trials. You'll bridge the gap between complex data programming and clinical development, ensuring that every statistical analysis meets the highest industry standards and drives our mission to defeat serious chronic diseases.

Your responsibilities will include

  • Leading the 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
  • Ensuring quality control and compliance of SDTM and ADaM deliverables, managing submission packages and TFL generation according to industry standards and Novo Nordisk specifications
  • Coordinating with stakeholders across R&D to facilitate open learning sessions and share clinical data science expertise after each submission
  • Providing critical input to authority-required documents including Risk Management Plans, Investigator's Brochures, and Development Safety Update Reports
  • Managing day-to-day trial execution, reviewing protocols and Statistical Analysis Plans, and contributing to the interpretation and communication of clinical trial results
  • Overseeing effective collaboration with CROs and vendors, ensuring inspection readiness documentation is maintained throughout the trial lifecycle
  • Driving innovation by identifying better practices, creating improvements in methods and collaboration, and presenting at global knowledge-sharing forums

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.

You'll join the Clinical Data Science Bangalore team, which has grown from a small start-up to one of the largest units in Global Business Services, Bangalore, and a key contributor to Novo Nordisk's clinical development portfolio. With decades of experience, our team brings together seasoned programmers and fresh perspectives to ensure high-quality statistical analysis and programming support for all clinical development activities worldwide—from early development phases to product introduction.

Your skills & qualifications

We're looking for an analytical thinker who thrives in a fast-paced, collaborative environment and can handle multiple priorities with precision. You'll bring:

  • Bachelor's or Master's degree in life sciences, natural sciences, engineering, or equivalent qualifications
  • 3-5 years of statistical programming experience, with preferably 1 year within the pharmaceutical industry or equivalent relevant experience
  • Extensive programming expertise in SAS or R, with proven experience in reporting clinical trials, including statistical data handling, analysis and reporting
  • Strong knowledge of drug development, clinical database technologies, data models, and advanced programming techniques
  • Experience with program review and documentation, along with in-depth understanding of GxP and guidelines within drug development
  • Excellent planning and coordination skills, with the ability to manage variable workloads and handle numerous tasks simultaneously while maintaining systematic organization
  • Outstanding communication skills in written and spoken English, with experience presenting to diverse audiences and collaborating across professional and regional borders
  • Personal qualities including independence, self-drive, strong analytical thinking, commitment, persistence, and the ability to seek innovative solutions while keeping things simple

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. In R&D, you'll experience a culture of continued learning that encourages you to expand your knowledge, work across different therapy areas, and collaborate with pioneers of science. When you join us, you're not just starting a job—you're becoming part of a story that spans generations.

Contact

To submit your application, please upload your CV online (click on Apply and follow the instructions).

Deadline

24th September, 2026

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

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.

Frequently Asked Questions

Where is the job located, and is it remote/hybrid/on-site?
The position is located in Bangalore (Bengaluru), Karnataka, India. The job posting does not specify a remote or hybrid work-mode policy.
What are the key responsibilities of this role?
You will lead clinical data science setup for trials, ensure quality control of SDTM and ADaM deliverables, coordinate with R&D stakeholders, provide input to authority-required documents, manage day-to-day trial execution, oversee CRO and vendor collaboration, and drive innovation in methods and collaboration.
What qualifications and experience do I need to apply?
You need a Bachelor's or Master's degree in life sciences, natural sciences, engineering, or equivalent. You also need 3-5 years of statistical programming experience (preferably 1 year in the pharma industry), extensive programming expertise in SAS or R, and strong knowledge of drug development, clinical database technologies, and GxP guidelines.
What is the application process and deadline?
To apply, you must upload your CV online by clicking 'Apply' and following the instructions. The application deadline is September 24th, 2026.

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Job Information

Source: manual
AI Relevance: 85/100 (Highly relevant)
Remote Type: onsite
Allowed Locations: Worldwide
Skills & Tags:
novo nordisk data science clinical
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