Novo Nordisk Global Business Services (GBS) India is inviting applications for the role of Associate Statistical Monitor at its Centralised Monitoring Unit (CMU) in Bangalore, Karnataka. This opportunity is ideal for freshers and early-career professionals (0–2 years) who are passionate about clinical trial data quality, centralized monitoring, and statistical data analysis.
If you are looking to build a career in clinical development, statistical monitoring, and GCP-compliant clinical research, this role offers exposure to global clinical trials and advanced data monitoring tools.
Job Overview
- Job Title: Associate Statistical Monitor
- Category: Clinical Development
- Location: Bangalore, Karnataka, India
- Department: Centralised Monitoring Unit (CMU), CDS GBS
- Company: Novo Nordisk Global Business Services (GBS) India
- Experience Required: 0–2 years
- Last Date to Apply: 15 January 2026
Key Responsibilities
As an Associate Statistical Monitor, you will be responsible for:
- Operating and maintaining the Statistical Monitoring function across clinical trials
- Detecting unusual data patterns, systematic errors, protocol deviations, and potential non-compliance or fraud
- Performing clinical trial data analysis and visualization
- Collaborating with trial teams and project stakeholders to plan and execute statistical monitoring activities
- Communicating findings to trial teams, management, and quality stakeholders
- Supporting the development of new statistical monitoring methods, tools, and training initiatives
- Contributing to continuous process improvement and data quality enhancement
- Participating in internal meetings, audits, and training programs
Eligibility Criteria & Qualifications
Candidates applying for the Associate Statistical Monitor job at Novo Nordisk should meet the following criteria:
Educational Qualification
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, Biostatistics, Engineering, or related disciplines
(B.Sc, M.Sc, B.Pharm, M.Pharm, MD, or equivalent)
Experience & Skills
- 0–2 years of experience in the pharmaceutical or clinical research industry
- Basic understanding of clinical research processes, GCP, and clinical data flow
- Foundational knowledge of statistical methods
- Exposure to clinical data reporting, visualization, or publications
- Working knowledge of SAS, JMP, or similar statistical tools
- Familiarity with GxP guidelines and regulated environments
- Strong analytical skills with a quality-focused mindset
- Ability to work independently and in cross-functional, global teams
About the Centralised Monitoring Unit (CMU)
The Centralised Monitoring Unit (CMU) at Novo Nordisk Bangalore is part of the Clinical Drug Development function. The team includes:
- Medical Reviewers ensuring patient safety and protocol compliance
- Functional Programmers building advanced operational dashboards
- Statistical Monitors identifying data integrity and compliance risks
This multidisciplinary team plays a critical role in ensuring high-quality, reliable clinical trial outcomes.
Why Join Novo Nordisk?
- Work with a top 20 global healthcare company by market capitalization
- Exposure to global clinical development projects
- Strong emphasis on innovation, ethics, and patient safety
- Inclusive, collaborative, and learning-driven work culture
- Opportunity to contribute to therapies impacting millions of patients worldwide
Estimated Salary (India)
- ₹6,00,000 – ₹9,00,000 per annum
(Indicative CTC for early-career clinical data and statistical monitoring roles in Bangalore)
How to Apply
