Looking for a clinical research job in Bangalore with strong growth potential? Fortrea is hiring a Sr. Centralized Study Coordinator to support global clinical trials, study management, and investigator payments. This role is ideal for candidates with 2โ3 years of clinical research experience, strong knowledge of ICH-GCP guidelines, and exposure to systems like CTMS, EDC, and eTMF.
If you’re aiming to build a career in clinical trial operations, study coordination, and data management, this opportunity offers hands-on exposure to end-to-end clinical study workflows.
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Job Overview
- Job Title: Sr. Centralized Study Coordinator
- Location: Bangalore, India
- Experience Required: 2โ3 Years
- Qualification: Life Sciences / Allied Health
- Job Type: Full-Time
- Last Date to Apply: June 30, 2026
Key Responsibilities
Clinical Systems & Study Management
- Manage clinical systems including CTMS, IWRS, and EDC
- Perform study system setup for new projects
- Handle access management across study platforms
- Ensure CTMS compliance and documentation accuracy
Data Review & Study Support
- Support data review activities and resolve queries with CRAs
- Generate study-specific reports
- Assist in study database maintenance
- Track and report study metrics and KPIs
eTMF & Documentation
- Support eTMF management and document tracking
- Assist in investigator submission packages
- Ensure proper filing and compliance with GCP documentation standards
Investigator Payments
- Review EDC and contracts for payment readiness
- Generate invoices and process payment batches
- Handle invoice QC and reconciliation
- Coordinate approvals with Project Managers and CTLs
Study Operations Support
- Assist in site startup activities
- Manage project communications
- Support contract management and study uploads
- Ensure timely issue escalation and resolution
Qualifications Required
- Bachelorโs degree in Life Sciences / Pharmacy / Healthcare
- OR certification in Nursing / Medical Technology / Lab Technology
- Strong understanding of ICH-GCP guidelines
- Fluent in English (written & verbal)
Experience Required
- 2โ3 years in clinical research
- Experience with clinical trial systems (CTMS, EDC, IWRS)
- Strong skills in:
- Communication
- Attention to detail
- Team collaboration
- Documentation & compliance
Why Apply for This Role?
- Work on global clinical trials
- Gain exposure to end-to-end study lifecycle
- Develop expertise in clinical systems & data review
- Opportunity to grow in clinical operations & project management
- Competitive salary and structured career progression
Salary (Expected Range)
- โน6,00,000 โ โน9,00,000 per annum (CTC)
(Based on experience and industry standards in Bangalore)
How to Apply
