If you’re looking to advance your career in clinical data monitoring, centralized monitoring, and risk-based monitoring (RBM), this opportunity at Syneos Health offers a high-impact role in global clinical trials. As a Central Monitor II / Sr Central Monitor, you will work on advanced analytics, signal detection, and clinical data surveillance to improve patient safety and study quality.
This role is ideal for professionals with experience in clinical research, pharmacovigilance, or clinical data management, aiming to transition into centralized monitoring and analytics-driven trial oversight.
Key Responsibilities โ Central Monitor Job
- Perform centralized clinical data surveillance using analytics and signal detection tools
- Analyze Quality Tolerance Limits (QTLs), Key Risk Indicators (KRIs), and SAE data
- Review study, site, and patient-level data for safety signals and protocol deviations
- Collaborate with cross-functional teams to develop dashboards, reports, and monitoring tools
- Manage queries, listings, edit checks, and compliance tracking
- Support audit readiness and regulatory compliance reporting
- Participate in risk assessment discussions and data review meetings
- Drive process improvements using predictive insights and analytics
- Ensure site-level database readiness and metric compliance
- Work closely with Clinical Data Surveillance Lead for delegated tasks
Qualifications Required
- Bachelorโs or Masterโs degree in Life Sciences, Pharmacy, Clinical Research, or related field
- Experience in clinical trials, centralized monitoring, or data analytics
- Strong knowledge of:
- Risk-Based Monitoring (RBM)
- Clinical trial data systems
- Safety data (SAE/AE analysis)
- Proficiency in data interpretation and analytical tools
- Excellent communication and cross-functional collaboration skills
Preferred Skills (High Ranking Keywords)
- Centralized Monitoring Analyst experience
- Clinical Data Surveillance / RBM expertise
- Knowledge of ICH-GCP guidelines
- Experience with clinical dashboards, QTLs, KRIs
- Understanding of clinical trial risk management and audit readiness
Salary (Estimated INR Range)
๐ฐ โน8,00,000 โ โน18,00,000 per annum (based on experience and seniority)
Benefits of Working at Syneos Health
- Global exposure to top pharmaceutical and biotech clinical trials
- Strong career development and progression programs
- Advanced training in clinical analytics and monitoring tools
- Inclusive and collaborative work culture
- Opportunity to work on innovative drug development programs
Job Location
๐ Hyderabad (Office-Based)
๐ Salem (India)
Why This Role is High Demand
With the increasing adoption of Risk-Based Monitoring (RBM) and AI-driven clinical trial analytics, roles like Central Monitor II are becoming critical in modern clinical research. Companies are shifting from traditional CRA monitoring to data-driven centralized monitoring models, making this a future-proof career path.
How to Apply
