Looking to build a career in clinical research and centralized monitoring? IQVIA is actively hiring for the role of Centralized Monitoring Assistant in Thane and Pune, Maharashtra. This is an excellent opportunity for life sciences graduates with clinical research experience to join a globally recognized CRO and work on cutting-edge clinical trials.
With increasing demand for risk-based monitoring (RBM) and central monitoring roles in India, this position offers strong career growth, hands-on exposure to study analytics, and collaboration with global teams.
Job Overview โ Centralized Monitoring Assistant
- Company: IQVIA
- Job Role: Centralized Monitoring Assistant
- Locations: Thane, Maharashtra | Pune, Maharashtra
- Job Type: Full-Time
- Experience Required: Minimum 2 years (including 6 months relevant experience)
- Application Deadline: May 2, 2026
This role involves supporting clinical study teams by performing centralized monitoring activities, analyzing site-level risk indicators (KRIs), and ensuring compliance with ICH-GCP guidelines.
Key Responsibilities
As a Centralized Monitoring Assistant, you will:
- Provide administrative and project-level support to clinical study teams
- Generate and manage study trackers, reports, and dashboards
- Assist in maintaining systems and ensuring data accuracy for analysis
- Support preparation of i-site packs and study documentation
- Perform access management tasks and coordinate with vendors
- Monitor Key Risk Indicators (KRIs) and site performance trends
- Identify site-level risks/issues early during study conduct
- Recommend corrective and preventive actions (CAPA)
- Evaluate effectiveness of monitoring actions
- Participate in kick-off meetings, client calls, and weekly updates
- Ensure compliance with SOPs, protocols, and regulatory requirements
Eligibility & Qualifications
To apply for this central monitoring job in India, candidates must have:
- Education: Graduate/Postgraduate in Life Sciences (B.Pharm, M.Pharm, BSc, MSc, etc.)
- Experience: Minimum 2 years total experience with at least 6 months in relevant clinical research role
- Basic knowledge of ICH-GCP (International Conference on Harmonisation โ Good Clinical Practice)
- Proficiency in Microsoft Excel, Word, and PowerPoint
- Strong communication and analytical skills
- Ability to manage timelines and work in a cross-functional environment
Preferred Skills
- Understanding of risk-based monitoring (RBM)
- Experience in clinical trial data review and site performance monitoring
- Strong attention to detail and data interpretation skills
- Ability to collaborate with global stakeholders
Salary & Benefits (Estimated)
- Salary Range: โน4.5 LPA โ โน7.5 LPA (based on experience)
- Exposure to global clinical trials and technologies
- Career growth in clinical operations and centralized monitoring
- Opportunity to work with a leading CRO (Contract Research Organization)
- Training in advanced clinical analytics and compliance frameworks
Why Join IQVIA?
IQVIA is a global leader in clinical research services, healthcare intelligence, and analytics. Working here means contributing to the development of innovative treatments while gaining experience in data-driven clinical trial monitoring.
How to Apply
