Novartis, a global leader in innovative medicines, is hiring an experienced Central Monitor (CM) for its Hyderabad office. This full-time role is part of Novartis’ Risk-Based Quality Management (RBQM) framework and plays a critical role in centralized monitoring, data surveillance, and clinical trial risk management.
If you have strong experience in clinical trial monitoring, KRIs, QTLs, and GCP, this opportunity offers a chance to work closely with global clinical teams and advanced central monitoring technologies.
Key Job Details
- Job Title: Central Monitor
- Job ID: REQ-10070501
- Location: Hyderabad, India (Office-based)
- Employment Type: Full Time
- Department: Global Clinical Operations / Data Surveillance
- Last Date to Apply: 20 February 2026
Role Overview – Central Monitor (CM)
The Central Monitor supports clinical trial oversight through centralized data monitoring and analytics-driven risk detection. The role involves early and continuous engagement across the trial lifecycle, working with Risk Surveillance Leads (RSLs), Data Analysts, and Clinical Trial Teams (CTTs) to proactively identify and mitigate risks related to patient safety, data quality, and protocol compliance.
This position is ideal for professionals with hands-on experience in central monitoring platforms, KRIs review, RBQM strategies, and adaptive monitoring models.
Key Responsibilities
Central Monitoring Execution
- Execute centralized monitoring strategies across clinical trials
- Perform ongoing data surveillance to identify trends, anomalies, and risk signals
- Review central monitoring technology outputs with Data Analysts
- Ensure compliance with RBM plans, SOPs, and GCP standards
Risk Identification & Management
- Identify site-level and study-level risks aligned with IQRMP
- Support risk assessment, root cause analysis, and CAPA recommendations
- Design, review, and optimize Key Risk Indicators (KRIs) and thresholds
- Monitor Quality Tolerance Limits (QTLs)
Cross-Functional Collaboration
- Act as CM point of contact for assigned studies
- Work closely with RSLs, Study Leaders, Data Managers, and Clinical Scientists
- Participate in Clinical Trial Team (CTT) meetings with data-driven insights
- Develop and maintain the Trial Monitoring Plan (TMP)
Documentation & Compliance
- Document findings and escalate critical risks promptly
- Ensure inspection-ready documentation
- Support continuous improvement initiatives in centralized monitoring
Essential Qualifications & Experience
- University degree in Life Sciences, Business, or Operations
- ≥5 years experience in pharmaceutical industry or CROs
- ≥3 years hands-on experience in clinical monitoring (central or site)
- Strong expertise in:
- Central Monitoring & KRIs
- RBQM and adaptive monitoring
- GCP / ICH guidelines
- Clinical trial risk management
- Experience with clinical data analytics or data management is an advantage
- Excellent analytical, critical thinking, and communication skills
- Fluent in written and spoken English
Why Join Novartis?
- Work on global, high-impact clinical trials
- Exposure to advanced central monitoring technologies
- Strong culture of diversity, inclusion, and compliance
- Career growth in RBQM, data-driven monitoring, and clinical operations
- Collaborative environment with global stakeholders
Estimated Salary Range (India)
💰 ₹18,00,000 – ₹28,00,000 per annum
(Indicative range based on industry standards for Central Monitoring roles in Hyderabad)
How to Apply
