Novo Nordisk is hiring a Central Monitor in Bangalore, Karnataka as part of its Global Business Services – Centralised Monitoring Unit (CMU). This opportunity is ideal for clinical research professionals with experience in risk-based quality management (RBQM), clinical trial monitoring, data analytics, and ICH-GCP compliance.
The Central Monitor role focuses on improving clinical trial quality through centralised operational monitoring, identifying potential risks affecting patient safety, data quality, and regulatory compliance. Candidates with experience in clinical operations, CRA monitoring, clinical data review, and analytics-driven decision-making are encouraged to apply.
Job Details
- Company: Novo Nordisk
- Job Role: Central Monitor
- Department: Centralised Monitoring Unit (CMU), Global Trial Portfolio
- Location: Bangalore, Karnataka, India
- Employment Type: Full-Time
- Category: Clinical Development
- Experience Required: 3+ years in clinical research
- Application Deadline: 23 July 2026
About the Central Monitor Role
A Central Monitor supports clinical trial oversight by reviewing operational data, analysing risk indicators, and ensuring trials are conducted according to protocol requirements, ICH-GCP guidelines, and regulatory expectations.
The role combines clinical research expertise with data analytics and technology-driven monitoring approaches. The Central Monitor works closely with global stakeholders, medical reviewers, statistical monitors, functional programmers, and clinical trial teams.
Key Responsibilities of Central Monitor at Novo Nordisk
The selected candidate will be responsible for:
- Performing ongoing centralised operational monitoring activities for assigned clinical studies.
- Reviewing vendor platform dashboards and monitoring outputs according to Novo Nordisk SOPs and regulatory guidelines.
- Defining and reviewing Key Risk Indicators (KRIs) impacting patient safety, data quality, and compliance.
- Supporting risk-based monitoring (RBM) strategies for clinical trials.
- Using data visualisation and analytics tools to identify operational risks and trends.
- Providing insights from aggregate clinical trial data reviews.
- Supporting applications, databases, and systems used for clinical monitoring.
- Communicating monitoring findings with cross-functional stakeholders.
- Participating in project meetings and contributing to continuous improvement initiatives.
- Maintaining compliance with ICH-GCP E6(R2), E6(R3), SOPs, and regulatory requirements.
Required Qualifications and Skills
Candidates applying for this Central Monitor job in Bangalore should have:
- Bachelor’s degree or higher in life sciences, healthcare, pharmacy, or scientific disciplines.
- Minimum 3 years of clinical research experience.
- Strong understanding of the drug development process and clinical trial operations.
- Experience applying RBQM principles in clinical trials.
- Knowledge of ICH-GCP E6(R2) and E6(R3) guidelines.
- Understanding of clinical trial design, execution, and monitoring processes.
- Experience in aggregate data review and interpretation.
- Familiarity with data visualisation and analytics platforms.
- Basic understanding of AI applications in clinical operations.
- Strong communication, presentation, and stakeholder management skills.
Preferred Skills
Candidates with the following experience will have an advantage:
- Previous CRA (Clinical Research Associate) or field monitoring experience.
- Experience with central monitoring platforms.
- Knowledge of CluePoints solutions.
- Experience working with global clinical trial teams.
Salary Range for Central Monitor Role in India
The estimated salary range for a Central Monitor role at Novo Nordisk Bangalore is approximately:
₹8,00,000 – ₹15,00,000 per annum
The final compensation may vary depending on experience, qualifications, and company policies.
Why Join Novo Nordisk?
Novo Nordisk provides opportunities to work in a global clinical development environment focused on innovation and patient outcomes.
Benefits of joining include:
- Opportunity to work with global clinical research teams.
- Exposure to advanced clinical monitoring technologies.
- Career growth in clinical development and RBQM.
- Learning opportunities in AI-enabled clinical operations.
- Experience with global pharmaceutical research practices.
- Inclusive and collaborative workplace culture.
How to Apply
