IQVIA India is hiring a Centralized Monitoring Assistant in Bengaluru for professionals with experience in clinical research, centralized monitoring, CRC, or CTA roles. This is a full-time, hybrid opportunity to work on global clinical trials while supporting risk-based monitoring, site oversight, and data integrity in accordance with ICH-GCP and regulatory standards.
If you are looking to grow your career in centralized monitoring jobs in India, this role offers strong exposure to analytics-driven monitoring, cross-functional collaboration, and global study delivery.
🔍 Job Overview
- Role: Centralized Monitoring Assistant
- Company: IQVIA India
- Location: Bengaluru, Karnataka
- Work Mode: Hybrid (General Shift)
- Job Type: Full-time
The Centralized Monitoring Assistant supports centralized monitoring activities across assigned studies, ensuring high-quality and compliant execution of clinical trials.
🧩 Key Responsibilities
- Oversee clinical deliverables from study start-up to close-out
- Support centralized monitors in identifying risks and resolving issues
- Review Site Visit Reports (SVRs) for quality and compliance
- Assist in monitoring strategy development and risk mitigation planning
- Track study metrics, trends, and performance indicators
- Manage site performance and operational triggers
- Ensure compliance with Central Monitoring Plans (CMPs)
- Support unblinded monitoring and investigational product (IP) management when applicable
- Maintain accurate documentation and audit readiness
- Contribute to training activities and continuous process improvement
- Assist with finance-related study data and investigator payments
🎓 Qualifications & Experience
- Bachelor’s degree in Life Sciences / Medical / Scientific discipline
- OR Medical degree with relevant clinical research experience
- Minimum Experience: 1–5 years as CRC, CTA, or in centralized monitoring
- Strong understanding of ICH-GCP, regulatory requirements, and protocols
- Good knowledge of clinical data and monitoring processes
- Excellent communication and organizational skills
💼 Preferred Skills
- Centralized Monitoring experience
- Risk-Based Monitoring (RBM)
- Clinical trial systems & analytics tools
- Issue management & trend analysis
- Cross-functional collaboration
💰 Salary (Estimated)
₹4,50,000 – ₹9,00,000 per annum (based on experience & skill set)
🌟 Why Join IQVIA?
- Global exposure to large-scale clinical trials
- Hybrid working model
- Strong learning and career growth opportunities
- Work with industry-leading clinical research professionals
- Inclusive and innovation-driven work culture
📥 How to Apply
