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Fortrea is urgently hiring Centralized Study Analysts (2 openings) for its Bangalore location (remote flexibility available). This role is ideal for candidates with 3โ5 years of clinical research experience, especially those skilled in eTMF, CTMS, EDC, and clinical trial operations.
If you are aiming to build a career in clinical data management, study operations, and trial support, this is a high-impact opportunity with a global CRO.
โณ Deadline: March 24, 2026 (Apply within hours)
๐งช Key Responsibilities โ Centralized Study Analyst
๐ Clinical Systems & Study Management
- Manage clinical systems (CTMS, IWRS, EDC)
- Handle access management and system setup
- Maintain study databases and compliance tracking
๐ eTMF & Document Management
- Support eTMF filing and document tracking
- Review investigator packages and informed consent forms (ICF)
- Ensure compliance with ICH-GCP and regulatory guidelines
๐ Data Review & Reporting
- Perform study-level data review and follow-ups with CRAs
- Generate study reports and analytics
- Resolve data discrepancies and outstanding queries
๐ค Study Coordination & Communication
- Manage internal/external communication
- Track CRA activities and action items
- Support study teams in daily operations
๐ฐ Investigator Payments & Budget Tracking
- Process site/vendor payments via CTMS
- Handle invoice QC, reconciliation, and approvals
- Manage pass-through expenses and payment batches
๐ฏ Eligibility Criteria
๐ Qualification
- Life Sciences / Pharmacy / Nursing / Medical degree (preferred)
๐ Experience
- 3โ5 years in clinical research
- Strong understanding of:
- ICH-GCP guidelines
- eTMF, CTMS, EDC systems
- Clinical trial processes
๐ง Skills Required
- High attention to detail
- Strong communication & coordination
- Ability to manage multiple study tasks
- Proficiency in clinical systems & MS Office
๐ผ Why This Role Matters
This Centralized Study Analyst role sits at the core of clinical trial execution, bridging:
- Clinical operations
- Data management
- Regulatory compliance
It gives exposure to global trials, sponsor communication, and end-to-end study lifecycle, making it a strong career move toward:
- Clinical Project Manager
- Study Lead
- Data Management Lead
๐ฐ Salary (Estimated)
- โน6 LPA โ โน10 LPA (based on experience & CRO standards)
๐ Benefits
- Work with a global CRO (Fortrea)
- Remote / hybrid flexibility
- Exposure to international clinical trials
- Strong career growth in CDM & study operations
- Learning across CTMS, eTMF, and regulatory workflows
๐ฉ How to Apply
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