Introduction Paragraph Fortrea is hiring a Central Monitor Assistant for its Clinical Research team in Bangalore. This full-time role is ideal for candidates with 2-3 years of clinical research experience. Excellent opportunity to join a global leader in clinical development and life sciences services.
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About the Company
Fortrea is a leading global contract research organization (CRO) providing clinical development and commercialization services to the life sciences industry.
With a strong focus on innovation, quality, and patient outcomes, Fortrea supports biotech and pharmaceutical companies in bringing new therapies to market efficiently. The company offers a dynamic, collaborative work environment with excellent professional growth opportunities.
Job Details
- Company Name: Fortrea
- Position: Central Monitor Assistant
- Department: Clinical & Medical / Research
- Experience: 2-3 Years in Clinical Research
- Location: Bangalore, Karnataka
- Work Type: Full-time (Hybrid/Office-based)
Job Description
Fortrea is seeking a detail-oriented professional to provide crucial support to clinical study teams through data management, monitoring support, investigator payments, and system administration.
Central Monitor Assistant
- Department: Clinical Research / Study Support
- Role: Central Monitor Assistant
- Qualification: University/College Degree (Life Science preferred) or Certification in allied health profession
- Experience: 2-3 Years in Clinical Research (ICH-GCP knowledge required)
- Location: Bangalore
Skills/Qualifications
- Strong working knowledge of ICH-GCP and clinical research guidelines
- Experience with clinical systems (CTMS, EDC, IWRS, e-TMF)
- Excellent organizational, communication, and multitasking skills
- Proficiency in Microsoft Excel and data handling
- Attention to detail and ability to work independently
Key Responsibilities
- Manage clinical systems access and study databases (CTMS, EDC, IWRS, etc.)
- Support e-TMF management, data review, and report generation
- Handle Investigator Payment processing and reconciliation
- Perform study system setup and CTMS compliance management
- Assist in document management and site startup activities
- Support Lead Monitors with data review and issue resolution
- Generate study-specific reports and maintain project documentation
- Participate in client/study team meetings and escalate issues timely
Benefits/Perks
- Opportunity to work with a global CRO leader
- Exposure to diverse clinical trials and therapeutic areas
- Professional development and learning opportunities
- Collaborative and inclusive work culture
- Competitive compensation and benefits
How to Apply
Interested candidates can apply directly through the Fortrea careers portal using Job Requisition ID: 262504.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Fortrea Career page.
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For more clinical research jobs, CRO jobs, and pharma jobs in Bangalore, visit Pharma Recruiter.
Apply before the deadline (June 30, 2026) and take the next step in your clinical research career with Fortrea!
Why You Should Join
Fortrea offers a stimulating environment where you can contribute to meaningful clinical research while building expertise in study support and data management. As part of a global team, you will gain valuable experience across multiple clinical trials and enjoy strong career progression opportunities.
FAQs
What is the experience required for Central Monitor Assistant at Fortrea?
Minimum 2-3 years of experience in clinical research with good knowledge of ICH-GCP.
What educational qualification is needed?
University degree in Life Sciences or certification in allied health profession.
Is the role completely remote?
The position is based in Bangalore with possible hybrid flexibility.
What systems will I work with?
CTMS, EDC, IWRS, e-TMF, and other clinical trial management systems.
This is a strong opportunity for Clinical Research jobs, Central Monitoring roles, and CRO careers in Bangalore. Eligible candidates with relevant experience are encouraged to apply before June 30, 2026.
