Life Sciences Jobs | Novo Nordisk is Hiring | Apply Now
Looking for high-growth Life Sciences Jobs in the pharmaceutical and clinical research industry? A new Novo Nordisk Career opportunity has been announced for the position of Associate Senior Clinical Data Scientist in Bangalore. This role is ideal for professionals with expertise in clinical data management, statistical programming, SAS, R, and clinical trial data standards. Candidates seeking specialized CDM Jobs can leverage this opportunity to contribute to global clinical development programs while working with one of the world’s leading healthcare companies.
- Job Title: Associate Senior Clinical Data Scientist
- Category: Data & AI
- Location: Bangalore, Karnataka, IN
About the Company
Novo Nordisk is a global healthcare company with more than 100 years of experience in developing innovative treatments for chronic diseases. The organization focuses on improving patient outcomes through research, clinical development, data science, and advanced healthcare solutions. Through its Research & Development division, Novo Nordisk combines scientific expertise, human data, digital innovation, and artificial intelligence to develop transformative therapies for millions of patients worldwide.
Key Responsibilities
- 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
Qualifications
- 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
Skills and Requirements
- 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
This Novo Nordisk Career opportunity offers an excellent pathway for professionals interested in clinical development, data science, and regulatory programming. Candidates seeking advanced Life Sciences Jobs and specialized CDM Jobs can gain valuable exposure to global clinical trials, statistical programming, regulatory standards, and pharmaceutical research while contributing to innovative therapies that impact millions of patients worldwide.
