Healthcare Job at Fortrea in Bangalore
Fortrea is offering an excellent healthcare job opportunity for experienced clinical research professionals in Bangalore. This full-time role of Centralized Study Specialist is ideal for candidates seeking long-term growth in Fortrea jobs while working on global clinical trials. If you are exploring rewarding jobs in Bangalore within the healthcare and life sciences domain, this role provides strong exposure to clinical operations, study management, and cross-functional collaboration.
Healthcare Job Details:
- Job Title: Centralized Study Specialist I
- Location: Bangalore
- Time Type: Full-time
- End Date: January 31, 2026
- Job Requisition ID: 256139
About the Company
Fortrea is a global contract research organization (CRO) delivering end-to-end clinical development solutions to pharmaceutical and biotechnology companies. Known for operational excellence and regulatory compliance, Fortrea supports complex clinical trials worldwide. Professionals looking for stable healthcare jobs with global exposure often choose Fortrea jobs for long-term career development, especially in key hubs offering high-demand jobs in Bangalore.
Qualifications
- University/College Degree or allied health certification (Ex, Medical or laboratory technology)
- Minimum 3+ years of experience in clinical development or regulatory/start-up activities
- Familiarity with investigator start-up documents and budget negotiations preferred
- Previous interaction with operational project teams and investigative sites
- Working knowledge of ICH, RA, IRB/IEC regulations
- Understanding of clinical trial processes and ICH-GCP guidelines
Healthcare Job Description
This healthcare job of Centralized Study Specialist I at Fortrea involves managing centralized clinical study activities while ensuring adherence to SOPs, work instructions, and regulatory guidelines. The role supports study monitoring, reporting plans, clinical systems, and communication across teams, making it a critical position within Fortrea jobs in Bangalore’s growing clinical research ecosystem.
Key Responsibilities
- Follow all applicable departmental Standard Operating Procedures and Work Instructions.
- Complete day-to-day tasks, ensuring quality and productivity
- Execute high-quality, timely monitoring and reporting plans
- Track and report study metrics as required
- Identify and implement process improvement opportunities
- Mentor and train team members
- Manage clinical systems and study documentation, including eTMF
- Maintain study databases such as CTMS, IWRS, and EDC
- Track and follow up with CRAs for outstanding issues
- Support the generation of study-specific reports
- Manage internal and external communications
- Assist in training compliance for study teams
- Support study payments for sites and vendors
- Document and track study activities using project management tools
- Prepare CRA Prep Packs and coordinate with CRAs and clinical teams
- Address site-level issues and provide updates to clinical teams
- Maintain Trial Master File documentation and participate in TMF QC
- Support compliance metrics and overall project health
- Update timelines and milestones in MS Project and CTMS
- Assist Project Leads with study planning and execution
- Support vendor management, RIM changes, and system documentation
