IQVIA, one of the world’s leading Clinical Research Organizations (CROs), has announced recruitment for Centralized Site Assistant and Centralized Site Associate positions in Thane, Maharashtra. These opportunities are ideal for experienced life sciences professionals looking to build careers in centralized clinical operations, remote site monitoring, and clinical trial management.
Candidates with experience in Clinical Research, Clinical Trial Operations, Centralized Monitoring, EDC Systems, CTMS, ICH-GCP, and Microsoft Excel are encouraged to apply.
Job Overview
| Details | Information |
|---|---|
| Company | IQVIA |
| Job Roles | Centralized Site Assistant & Centralized Site Associate |
| Job Type | Full-Time |
| Location | Thane, Maharashtra, India |
| Experience | 2โ5 Years (Role Dependent) |
| Qualification | Graduate/Postgraduate in Life Sciences or Related Field |
| Last Date | 21 July 2026 |
Vacancy 1: Centralized Site Assistant
Key Responsibilities
- Support Clinical Study Management teams with administrative activities
- Prepare study reports and trackers
- Maintain project databases and compliance systems
- Generate study status reports
- Prepare i-site packs
- Support access management requests
- Assist Technical Solution Specialists using Microsoft Excel
- Review Key Risk Indicators (KRIs)
- Identify potential site risks
- Recommend corrective actions
- Participate in project meetings
- Support Central Monitoring activities
Eligibility
Applicants should possess:
- Graduate or Postgraduate degree in Life Sciences
- Minimum 2 years overall experience
- At least 6 months of relevant Clinical Research experience
- Knowledge of:
- ICH-GCP
- Clinical Research regulations
- Microsoft Excel
- Word
- PowerPoint
- Good communication skills
- Strong attention to detail
Vacancy 2: Centralized Site Associate
Key Responsibilities
- Perform centralized monitoring activities
- Review site quality and protocol compliance
- Monitor pending queries and SDV backlog
- Support Clinical Trial Management teams
- Review subject-level clinical data
- Perform clinical trend analysis
- Maintain CTMS, EDC and IXRS systems
- Review inclusion/exclusion criteria
- Review adverse events and SAEs
- Generate study analytics
- Identify operational risks
- Recommend monitoring actions
- Support study compliance
- Assist in automation using Excel macros
- Act as backup for Centralized Monitors
Eligibility
Candidates should have:
- Graduate/Postgraduate degree in Life Sciences
- 2โ5 years experience
- Minimum 1 year relevant Clinical Research experience
- Knowledge of:
- Electronic Data Capture (EDC)
- CTMS
- IXRS
- ICH-GCP
- Clinical Trial Operations
- Clinical Data Review
- Global Clinical Trials
- Strong Microsoft Excel skills
- Excellent communication skills
- Good analytical abilities
Preferred Skills
- Clinical Trial Management
- Centralized Monitoring
- Remote Site Monitoring
- Risk-Based Monitoring
- CTMS
- EDC Systems
- IXRS
- Microsoft Excel
- Clinical Analytics
- Study Tracking
- Clinical Documentation
- GCP Compliance
- Data Review
- Site Performance Monitoring
- Clinical Operations
Why Join IQVIA?
IQVIA is among the world’s largest healthcare intelligence and clinical research organizations, providing innovative solutions across drug development and commercialization.
Benefits include:
- Global Clinical Research exposure
- Career progression opportunities
- International project experience
- Learning & development programs
- Collaborative work environment
- Exposure to advanced clinical technologies
- Work with leading pharmaceutical sponsors
Salary (Expected)
Based on current market standards, the estimated annual salary is:
- Centralized Site Assistant: โน4 โ โน6.5 LPA
- Centralized Site Associate: โน7 โ โน11 LPA
Actual compensation depends on experience, skills, project allocation, and interview performance.
How to Apply
Application Link For Centralized Site Assistant
Application Link For Centralized Site Associate
