Work as Associate Senior Clinical Data Scientist at Novo Nordisk

Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy.

Post : Associate Senior Clinical Data Scientist

Your new role
As an Associate Senior Clinical Data Scientist, you'll be a key operational partner within trial squads, managing critical tasks across clinical trials and cross-trial activities that directly support our mission to defeat serious chronic diseases. Your technical expertise will ensure the highest quality standards in statistical programming and data management throughout the clinical development lifecycle.

Job Description
• Managing assigned tasks within clinical trials, including finalizing SDTM and ADaM deliverables, preparing and reviewing annotated CRFs (aCRFs), generating SDTM datasets, programming ADaM, and creating TFLs in compliance with regulatory standards
• Contributing to trial setup activities such as developing eCRFs, Data Flow Plans, metadata specifications, mock TFLs, SDRG, ADRG, and Define.xml
• Supporting Clinical Study Reports (CSRs), Risk Management Plans (RMP), Investigator Brochures (IB), Development Safety Update Reports (DSUR), Periodic Safety Update Reports (PSUR), and public disclosure deliverables
• Collaborating with internal and external stakeholders including CROs, regulatory authorities, and scientific communities to ensure seamless trial execution
• Sharing best practices, contributing to process optimization, and supporting change management initiatives that advance our data standards and programming practices
• Providing training and support for colleagues on statistical computing environments, system usage, and SOP understanding
• Ensuring all documentation and programming practices meet Good Clinical Practice (GCP), Good Documentation Practice (GDP), and Good Programming Practice (GPP) standards

Candidate Profile
• Bachelor's or Master's degree in life sciences, natural sciences, engineering, or equivalent qualifications
• 2-3 years of programming experience, preferably working with biological data or equivalent knowledge through relevant practical experience
• Proficiency in programming languages such as SAS or R
• Experience with clinical database technologies, data models, and advanced programming techniques
• Demonstrated ability to collaborate effectively across professional and regional borders in a multinational environment
• Strong analytical skills combined with independence, self-drive, and accountability in managing variable workloads
• Excellent communication skills with fluency in written and spoken English, and the ability to explain technical issues to both peers and stakeholders
• Basic understanding of the pharmaceutical industry and key elements of the clinical development value chain

Additional Information
Experience : 2-3 years
Qualification : Bachelor's or Master's degree in life sciences
Location : Bangalore, Karnataka
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Clinical Data Science
End Date : 25th September 2026