Novo Nordisk Careers: Apply Now for Central Monitor Role
Novo Nordisk Careers: Novo Nordisk India is hiring a Central Monitor for its Global Business Services (GBS) unit in Bengaluru. This role is ideal for clinical research professionals who thrive in a dynamic, data-driven environment and are passionate about patient safety, risk-based monitoring, and regulatory compliance. Join a global organization where innovation, collaboration, and continuous improvement are at the core of clinical development.
Novo Nordisk Careers: Job Details
- Job Title: Central Monitor
- Department: Centralised Monitoring Unit (CMU)
- Job Category: Clinical Development
- Location: Bengaluru, India
- Work Mode: On-site
- Employment Type: Full-time
About the Company
Novo Nordisk is a global healthcare leader focused on driving change in chronic disease management, particularly diabetes and other serious conditions. With a strong patient-first philosophy, Novo Nordisk combines cutting-edge science with an inclusive and purpose-driven work culture. Novo Nordisk India, through its Global Business Services (GBS), supports global clinical and operational activities, contributing significantly to innovation, compliance, and patient safety across worldwide clinical trials.
Novo Nordisk Careers: Qualifications
- Bachelor’s degree in healthcare or a Scientific discipline
- Minimum 3+ years of relevant clinical research experience
- Strong knowledge of drug development processes and Risk-Based Quality Management (RBQM)
- In-depth understanding of ICH-GCP E6 R2 & R3 guidelines
- Experience in centralized monitoring, clinical operations, or CRA/field monitoring preferred
- Proficiency in data visualization and analytics tools
- Experience with CluePoints or similar platforms is an advantage
- Basic understanding of AI tools in clinical operations
About the Role
As a Central Monitor, the role focuses on centralized operational monitoring of clinical trials with an emphasis on patient safety, data quality, and regulatory compliance. The position involves defining and tracking Key Risk Indicators (KRIs), analyzing trial data through advanced visualization tools, and collaborating closely with global stakeholders to proactively identify and mitigate operational risks.
Key Responsibilities
- Define and implement standard and trial-specific Key Risk Indicators (KRIs)
- Perform ongoing centralized operational monitoring using vendor dashboards and analytics tools
- Identify risks related to patient safety, data integrity, and protocol compliance
- Ensure monitoring activities align with NN SOPs, ICH-GCP, and regulatory guidelines
- Communicate monitoring findings to cross-functional stakeholders for informed decision-making
- Act as a primary contact for assigned centralized monitoring studies
- Participate in project meetings and contribute to trial oversight discussions
- Support continuous improvement initiatives and share best practices across CMU
- Maintain compliance with global and local SOPs and quality standards
