Novo Nordisk is hiring for the position of Clinical Data Insights Analyst at its Global Business Services operations in Bangalore, Karnataka. This opportunity falls under the Data & AI category within Research & Development and offers professionals an opportunity to work with global clinical trial data and advanced data review processes.
Candidates with a BSc or MSc in Natural Sciences/Life Sciences, a comparable degree in Medicine, or a Computer Science degree with equivalent professional experience can apply. Novo Nordisk preferably seeks candidates with 2+ years of Clinical Data Management experience, particularly within the pharmaceutical industry or drug development.
The Novo Nordisk Clinical Data Insights Analyst job is particularly relevant for candidates interested in clinical data management, risk-based data review, EDC/CDMS, clinical data visualization, UAT, database lock activities, data quality, and clinical research.
Novo Nordisk Clinical Data Insights Analyst – Job Overview
| Particular | Details |
|---|---|
| Company | Novo Nordisk |
| Role | Clinical Data Insights Analyst |
| Category | Data & AI |
| Department | Research & Development |
| Function | Clinical Data Management & Programming |
| Location | Bangalore, Karnataka, India |
| Qualification | BSc/MSc Natural/Life Science, Medicine or Computer Science |
| Experience | Preferably 2+ Years |
| Industry | Pharmaceutical / Clinical Research |
| Application Deadline | September 21, 2026 |
About the Clinical Data Insights Analyst Role
As a Clinical Data Insights Analyst, the selected candidate will work as a Data Management (DM) Trial Partner within the trial Data Management team.
The primary objective of this role is to ensure high-quality clinical trial data for analysis and regulatory submission. The analyst will plan and execute clinical data reviews, implement risk-based data management approaches, identify anomalies and trends, manage data queries, create data review specifications and communicate meaningful clinical data insights to stakeholders.
The position combines Clinical Data Management, data analytics, data visualization and clinical trial operations, making it particularly relevant for candidates seeking data-focused careers in pharmaceutical R&D.
Key Responsibilities
Selected candidates will be responsible for:
- Planning and coordinating clinical data review activities and assessing associated risks.
- Applying risk-based data management and risk-based data review methodologies.
- Developing specifications for clinical data review tools, reports and visualizations.
- Collaborating with programmers for system setup, User Acceptance Testing (UAT) and deployment.
- Reviewing clinical data across databases, datasets, listings, reports, analytics and visualizations.
- Assessing clinical trial data for completeness, accuracy and integrity.
- Raising, reviewing and closing queries through EDC/CDMS systems.
- Ensuring identified data issues are reviewed and appropriately corrected by qualified site personnel.
- Independently driving data review activities within the Clinical Data Review scope.
- Using data visualization techniques to identify and communicate meaningful findings.
- Analysing clinical data patterns and trends to identify potential anomalies.
- Communicating trending analyses and data review findings to relevant stakeholders.
- Supporting trial partners with insights for operational decision-making.
- Identifying potential site or CRA training requirements based on data findings.
- Maintaining productive relationships with Data Management trial partners and other stakeholders.
- Supporting clinical trial audits and regulatory inspections.
- Maintaining appropriate trial documentation and ensuring ongoing archival.
- Contributing to improvements in clinical data review processes, tools and methodologies.
- Verifying completion of data review activities with DM trial partners before database lock.
Qualifications – Who Can Apply?
Novo Nordisk specifies the following educational backgrounds:
BSc/MSc in Natural Sciences or Life Sciences, a comparable degree in Medicine, or a Computer Science degree with equivalent professional experience.
Depending on the exact degree curriculum and employer assessment, relevant Natural/Life Science backgrounds may include disciplines aligned with biological, biomedical or clinical sciences. Candidates should verify their individual degree eligibility against the official application requirements.
Experience Required
Novo Nordisk preferably requires 2+ years of Clinical Data Management experience, with the majority of that experience ideally gained within the pharmaceutical industry or drug development.
Therefore, this vacancy is primarily targeted toward candidates with prior clinical data management exposure rather than being explicitly advertised as a fresher position.
Skills Required
Candidates should have knowledge or experience across relevant areas such as:
- Clinical Data Management
- Clinical Data Review
- Risk-Based Data Management
- Risk-Based Data Review
- EDC/CDMS
- Clinical Trial Data
- Data Cleaning
- Data Visualization
- Data Analytics
- Data Trend Analysis
- User Acceptance Testing (UAT)
- Clinical Data Processing and Flow
- Database Lock
- Query Management
- Clinical Trial Methodology
- GCP
- Regulatory Requirements
- Audit & Inspection Readiness
- Stakeholder Management
Knowledge of clinical systems used during drug development and an understanding of how clinical data is collected, processed, reviewed and finalized are also important for this position.
Additional Competencies
Novo Nordisk is seeking candidates with effective written and verbal English communication skills, along with presentation and negotiation abilities.
Candidates should also demonstrate a team-oriented approach, flexibility, cross-cultural awareness and an ability to develop strong internal working relationships.
The role requires adaptability because clinical data processes, technologies and analytical approaches continue to evolve.
About the Department
The position is part of Research & Development, where scientific ideas are advanced into clinical testing with support from human data, technology and AI-driven approaches.
Within Clinical Data Management & Programming (CDM&P), employees contribute to delivering high-quality clinical trial data for evidence-based decision-making.
The global team works on technologies, systems and processes that support clinical development and ultimately the development of medicines for patients worldwide.
Why Consider This Novo Nordisk Opportunity?
The Novo Nordisk Clinical Data Insights Analyst job in Bangalore offers exposure to several high-value areas of modern clinical development, including:
- Global clinical trial data management
- Risk-based clinical data review
- Pharmaceutical R&D
- Clinical data analytics
- Data visualization
- EDC and clinical data management systems
- Clinical trial quality and compliance
- Cross-functional stakeholder collaboration
- Audit and inspection preparation
- Continuous development of clinical data tools and processes
Novo Nordisk also highlights professional learning and development opportunities as part of working for a global healthcare organization, with benefits designed around employees’ careers and life stages.
How to Apply


