Looking to build a career in clinical data monitoring and centralized surveillance? Syneos Health is hiring a Central Monitor II for candidates with 1โ3 years of experience in clinical data management, CTMS, and EDC systems. This is an excellent opportunity for life sciences graduates aiming to work in risk-based monitoring, data analytics, and clinical trial oversight.
This Central Monitor II job in India (Gurugram/Hyderabad, hybrid) offers exposure to advanced clinical data surveillance methodologies, dashboards, KRIs, QTLs, and signal detection, making it a high-growth role in the clinical research domain.
Job Overview
- Role: Central Monitor II
- Company: Syneos Health
- Experience: 1โ3 Years
- Location: Gurugram, Hyderabad (Hybrid)
- Employment Type: Full-Time
- Openings: 5
Key Responsibilities
As a Central Monitor II, you will play a crucial role in clinical trial data oversight and risk-based monitoring:
- Develop and maintain dashboards, reports, and analytics tools for clinical data review
- Perform centralized data surveillance and signal detection (QTLs, KRIs, SAEs)
- Review study, site, and patient-level clinical data for trends and deviations
- Manage queries, edit checks, listings, and compliance tracking
- Conduct vendor data reconciliation and audit trail reviews
- Support audit readiness and regulatory compliance activities
- Collaborate with cross-functional teams including data management and clinical operations
- Participate in risk assessments and data review meetings
- Contribute to process improvements and predictive risk identification
Required Qualifications
Educational Requirements
- Bachelorโs degree in Life Sciences, Health Sciences, Pharmacy, Biotechnology, or related field
Experience & Skills
- 1โ3 years of experience in:
- Clinical Data Management / Central Monitoring
- CTMS, EDC systems, Spotfire or similar tools
- Strong understanding of:
- GCP (Good Clinical Practice)
- Clinical data workflows and surveillance methodologies
- Hands-on exposure to:
- KRIs, QTLs, signal detection techniques
- Data visualization and analytics tools
- Skills:
- Analytical thinking & problem-solving
- Attention to detail
- Cross-functional communication
- Ability to manage multiple priorities
Preferred Skills
- Experience in user acceptance testing (UAT) and validation
- Knowledge of vendor data reconciliation
- Familiarity with clinical trial risk-based monitoring frameworks
Salary & Benefits
- Estimated Salary: โน4,00,000 โ โน8,00,000 per annum
- Hybrid work flexibility
- Exposure to global clinical trials and data analytics tools
- Career growth in clinical research, pharmacovigilance, and data science
- Opportunity to work with leading CRO (Contract Research Organization)
How to Apply
Application Link Through Naukri
