Global Clinical Research Organization (CRO) Fortrea has opened applications for two exciting opportunities in its Clinical Operations team:

• Centralized Study Coordinator
• Senior Centralized Study Coordinator

These positions are based in Bangalore and offer professionals an opportunity to work on global clinical trials, supporting study teams through clinical systems management, Trial Master File (TMF) activities, CTMS maintenance, vendor coordination, study documentation, and project tracking.

Candidates with experience in clinical trial operations, eTMF, CTMS, EDC, IWRS, clinical documentation, and study coordination are encouraged to apply.

Available Positions

1. Centralized Study Coordinator

Location: Bangalore, India

Employment Type: Full-Time

Company: Fortrea

2. Senior Centralized Study Coordinator

Location: Bangalore, India

Employment Type: Full-Time

Company: Fortrea

Key Responsibilities

Selected candidates will support global clinical studies by performing activities such as:

• Managing clinical systems and user access management
• Maintaining study documentation at study, country, and site levels
• Updating CTMS, IWRS, EDC, and other clinical databases
• Supporting electronic Trial Master File (eTMF) management
• Performing TMF quality control and archival activities
• Tracking study milestones, timelines, and project metrics
• Preparing CRA Prep Packs before monitoring visits
• Coordinating with CRAs to resolve outstanding site issues
• Supporting clinical data review activities
• Updating XRIM and project governance tools
• Tracking protocol deviations and action items
• Coordinating meetings and documenting meeting minutes
• Supporting vendor management activities
• Managing invoice trackers and purchase order requests
• Maintaining project documentation and compliance metrics
• Supporting project plans and study execution
• Participating in process improvements and SOP compliance
• Assisting study teams with cross-functional operational activities

Preferred Qualifications

Candidates with the following educational background are generally suitable for these positions:

• B.Pharm
• M.Pharm
• Pharm.D
• B.Sc Life Sciences
• M.Sc Life Sciences
• Biotechnology
• Clinical Research
• Nursing
• Biomedical Sciences
• Other relevant healthcare or life science qualifications

Desired Skills

Successful candidates should possess knowledge of:

• Clinical Trial Management System (CTMS)
• Electronic Trial Master File (eTMF)
• Electronic Data Capture (EDC)
• Interactive Web Response System (IWRS)
• Clinical Operations
• Trial documentation
• TMF Quality Control
• Clinical study coordination
• Vendor management
• Project coordination
• Risk management
• Protocol deviation tracking
• ICH-GCP guidelines
• Clinical documentation compliance
• Cross-functional collaboration

Why Join Fortrea?

Fortrea is one of the world’s leading Contract Research Organizations (CROs), offering professionals the opportunity to contribute to global clinical research programs while working with advanced clinical technologies and experienced multidisciplinary teams.

Benefits include:

• Global clinical research exposure
• Career progression within Clinical Operations
• International study experience
• Collaborative work environment
• Opportunity to work with advanced clinical systems
• Exposure to multinational sponsors
• Strong learning and development opportunities

How to Apply

Application Link For Centralized Study Coordinator

Application Link For Senior Centralized Study Coordinator