Clinical Research Jobs – Central Monitor at Novo Nordisk | Life Science Jobs | Apply Now
Are you searching for impactful clinical research jobs that combine innovation, patient safety, and global exposure? Novo Nordisk jobs offer life science professionals the chance to work in a dynamic clinical development environment. This Central Monitor role in Bangalore is ideal for candidates passionate about risk-based monitoring, clinical trial oversight, and advancing healthcare outcomes—making it a standout opportunity among life science jobs in India.
- Job Title: Central Monitor
- Category: Clinical Development
- Department: Centralised Monitoring Unit (CMU)
- Location: Bengaluru
About the Company:
Novo Nordisk is a global healthcare company driven by a strong purpose—putting patients first. With millions worldwide relying on its therapies, Novo Nordisk continues to lead innovation in diabetes care and clinical research. Working at Novo Nordisk means contributing to meaningful scientific progress while growing in a collaborative, international environment.
Job Overview:
The Central Monitor position within the Centralized Monitoring Unit (CMU) in Bangalore focuses on proactive, risk-based clinical trial monitoring. The role supports patient safety, data quality, and regulatory compliance through advanced analytics and close collaboration with global stakeholders.
Educational Requirements:
- Bachelor’s degree in life sciences, scientific, or healthcare discipline
- Minimum 3+ years of relevant clinical research experience
- Strong understanding of drug development and RBQM principles
Key Responsibilities:
- Define and monitor trial-specific and standard Key Risk Indicators (KRIs)
- Perform ongoing centralized operational monitoring using dashboards and analytics tools
- Identify risks related to patient safety, data quality, and compliance
- Communicate findings to stakeholders and participate in project meetings
- Ensure adherence to ICH-GCP, SOPs, and regulatory guidelines
- Drive continuous improvement and innovation within the CMU team
Skills Required:
- In-depth knowledge of ICH-GCP E6 R2/R3 guidelines
- Experience in risk-based quality management (RBQM)
- Strong analytical and data visualization skills
- Understanding of clinical trial operations and execution
- Excellent communication and stakeholder management abilities
- Ability to manage multiple priorities under tight deadlines
- Quality mindset with attention to detail
- Basic understanding of AI tools in clinical operations
- Experience with CluePoints solutions (preferred)
This Central Monitor role is a compelling opportunity for professionals seeking meaningful clinical research jobs with global impact. At Novo Nordisk, your expertise directly contributes to patient safety, innovation, and the future of clinical development, making this one of the most rewarding life science jobs available today.
