Looking to build a career in centralized monitoring, RBQM (Risk-Based Quality Management), and clinical data analytics?
Syneos Health is hiring a Central Monitor II (Remote โ India), offering an excellent opportunity for professionals in clinical research, pharmacovigilance, and data monitoring roles.
This role is ideal for candidates with experience in clinical trials, centralized monitoring, and data quality oversight, aiming to transition into advanced risk-based monitoring (RBM) functions.
๐ Job Details
- Position: Central Monitor II
- Company: Syneos Health
- Location: Remote (India)
- Job Type: Full-Time
- Mode: Remote (Exception-based)
- Posted On: March 17, 2026
- Last Date to Apply: March 19, 2026
๐ง Key Responsibilities (Central Monitoring / RBQM Role)
The Central Monitor II will play a critical role in clinical trial data oversight and risk-based monitoring:
- Support Central Monitoring Lead in RBQM tool setup and maintenance
- Perform centralized monitoring of clinical trial data
- Conduct data risk review and issue management using RBM tools
- Identify data trends, protocol deviations, and site-level risks
- Analyze study, country, and site performance metrics
- Communicate findings and recommend corrective actions to study teams
- Ensure documentation, compliance, and audit readiness
- Train study teams on central monitoring and RBQM processes
๐ Strong focus on data-driven clinical trial monitoring and analytics
๐ Eligibility & Qualifications
Educational Qualification
Candidates from life sciences and clinical research backgrounds can apply:
- B.Pharm / M.Pharm
- PharmD
- BSc / MSc (Life Sciences, Biotechnology, Microbiology)
- Clinical Research or related fields
Experience Required
- Typically 2โ5 years of experience in:
- Clinical Research (CRA, CTA, Data Management)
- Central Monitoring / RBM / RBQM
- Clinical Data Review or Risk-Based Monitoring
Required Skills
- Knowledge of RBQM (Risk-Based Quality Management)
- Experience with clinical data analytics tools
- Understanding of ICH-GCP guidelines
- Strong data analysis and interpretation skills
- Experience in clinical trial monitoring & compliance
- Excellent communication and stakeholder management
๐ฐ Salary (Estimated Range โ India)
- โน6 LPA โ โน12 LPA (Based on experience and company standards)
๐ Why Join Syneos Health?
- Work with a top global CRO involved in:
- 94% of FDA-approved drugs
- 95% of EMA-approved products
- Exposure to global clinical trials & RBQM frameworks
- Strong career growth in centralized monitoring & analytics
- Flexible remote working model
- Learning environment with advanced clinical technologies
๐ Career Scope
This role is highly valuable for transitioning into:
- Central Monitoring Lead
- Risk-Based Monitoring Specialist
- Clinical Data Analytics Expert
- Clinical Project Manager
๐ How to Apply
