Job Title: Central Monitor
Company: Novo Nordisk
Location: Bangalore, Karnataka, India
Employment Type: Full-time
Department: Centralised Monitoring Unit (Global Business Services)
Experience Required: 3+ years of experience in Clinical Research, Clinical Monitoring, or Risk-Based Quality Management (RBQM), preferably with CRA/Field Monitoring experience.
Education: Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Medical Sciences, or a related healthcare discipline.
Salary Package: ₹12–18 LPA (Estimated as per current market standards; final compensation depends on experience, skills, and interview performance.)
Key Responsibilities:
Perform centralized operational monitoring for assigned clinical studies.
Define and monitor Key Risk Indicators (KRIs) for patient safety, data quality, and regulatory compliance.
Conduct ongoing risk-based monitoring using dashboards and vendor platforms.
Utilize data visualization and analytics tools to identify study risks and trends.
Review and interpret operational clinical trial data.
Support applications, databases, and systems used for centralized monitoring.
Communicate monitoring findings and recommendations to project stakeholders.
Participate in project meetings as the primary Central Monitoring representative.
Ensure compliance with ICH-GCP, SOPs, and regulatory requirements.
Drive continuous improvement initiatives and share best practices across teams.
Required Skills:
Centralized Monitoring
Risk-Based Quality Management (RBQM)
Clinical Trial Monitoring
Key Risk Indicators (KRIs)
Clinical Operations
ICH-GCP E6 R2/R3
Clinical Trial Data Review
Data Visualization & Analytics
Risk Assessment
Clinical Research
Regulatory Compliance
Microsoft Office
Analytical & Problem-Solving Skills
Stakeholder Management
Communication & Presentation Skills
Preferred Skills:
CRA (Clinical Research Associate) or Field Monitoring experience.
Hands-on experience with CluePoints or similar centralized monitoring platforms.
Knowledge of AI tools in clinical operations.
Experience with operational dashboards and clinical data analytics.
Strong understanding of clinical trial design and execution.
Work Mode: Office-Based (Bangalore)
Benefits:
Competitive salary with performance-based growth.
Career development and continuous learning opportunities.
Exposure to global clinical trials and innovative technologies.
Collaborative and inclusive work culture.
Opportunity to work with one of the world's leading pharmaceutical companies.
Strong employee benefits and long-term career growth.
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