Clinical Monitor Job at Novo Nordisk
Looking for a Clinical Monitor Job with one of the world’s leading pharmaceutical companies? Novo Nordisk Careers is hiring a Central Monitor for its Global Business Services team in Bangalore, Karnataka. This opportunity is ideal for professionals with clinical research experience and expertise in Risk-Based Quality Management (RBQM), Good Clinical Practice (GCP), and clinical trial monitoring. If you’re looking to advance your career in Clinical Research Jobs in India, this role offers the chance to work on global clinical development programs that improve patient outcomes worldwide.
About Novo Nordisk:
Novo Nordisk is a global healthcare company with more than 100 years of innovation in treating chronic diseases. Dedicated to improving the lives of millions of people, the company develops breakthrough therapies in diabetes, obesity, rare diseases, and other serious chronic conditions. Through scientific excellence, digital innovation, and patient-focused research, Novo Nordisk continues to shape the future of healthcare across the globe.
The company’s Global Business Services division in Bangalore plays a critical role in supporting worldwide clinical development. Its Centralised Monitoring Unit (CMU) combines medical reviewers, statistical monitors, and technical experts to ensure patient safety, maintain data quality, and strengthen risk-based monitoring across global clinical trials.
Job Details:
- Job Title: Central Monitor
- Primary Keyphrase: Clinical Monitor Job
- Category: Clinical Development
- Department: Global Business Services, India
- Location: Bangalore, Karnataka, India
- Employment Type: Full-Time
Key Responsibilities:
- Perform centralized operational monitoring activities for assigned clinical studies.
- Define and monitor standard and trial-specific Key Risk Indicators (KRIs).
- Identify operational risks affecting patient safety, regulatory compliance, and data quality.
- Analyze operational data using visualization dashboards and advanced analytics tools.
- Support applications, databases, and systems used for centralized monitoring.
- Communicate monitoring findings and risk assessments to key stakeholders.
- Participate in project meetings and support cross-functional clinical trial teams.
- Ensure compliance with Novo Nordisk SOPs, ICH-GCP guidelines, and regulatory requirements.
- Promote continuous improvement, innovation, and best practices across the department.
- Contribute to Risk-Based Quality Management (RBQM) activities throughout clinical development.
Educational Qualification for the Clinical Monitor Job:
Candidates should possess:
- Bachelor’s degree in Healthcare or another discipline.
Experience Required:
Applicants should have:
- Minimum 3 years of clinical research experience.
- Strong understanding of drug development processes and clinical trial operations.
- Experience applying Risk-Based Quality Management (RBQM) principles.
- Knowledge of ICH-GCP E6 R2/R3 guidelines.
- Experience with data visualisation and operational analytics tools.
- Prior CRA or field monitoring experience is an added advantage.
- Experience with CluePoints solutions is desirable.
Required Skills for the Clinical Monitor Job:
- Clinical trial monitoring
- Risk-Based Quality Management (RBQM)
- Good Clinical Practice (ICH-GCP)
- Clinical data analysis
- Risk assessment and mitigation
- Data visualization and analytics
- Clinical operations
- AI tools in clinical research
- Stakeholder communication
- Cross-functional collaboration
- Problem-solving and analytical thinking
- Time management and multitasking
- Attention to detail
Important Details:
- Application Deadline: 23 July 2026
