Fortrea is inviting applications for the position of Centralized Study Analyst in Bangalore, India. This hybrid clinical research opportunity is ideal for professionals with 3–5 years of clinical research experience who have expertise in CTMS, eTMF, study documentation, investigator payments, study support, and ICH-GCP compliance.

If you’re looking to advance your career in Clinical Operations, Clinical Trial Management, Study Coordination, or Clinical Trial Support, this Fortrea job offers the opportunity to work on global clinical studies while collaborating with cross-functional teams.

Job Details

Primary Keywords

• Centralized Study Analyst Jobs
• Fortrea Careers
• Clinical Research Jobs Bangalore
• CTMS Jobs India
• eTMF Jobs
• Clinical Trial Support Jobs
• Clinical Operations Jobs
• Study Management Jobs
• Investigator Payments Jobs
• Clinical Study Analyst Jobs

About the Role

The Centralized Study Analyst at Fortrea supports global clinical trials by managing study systems, reviewing regulatory documentation, maintaining clinical databases, coordinating investigator payments, and ensuring compliance with ICH-GCP guidelines.

The role requires strong organizational skills, excellent documentation practices, and experience with clinical trial systems such as CTMS, EDC, IWRS, and eTMF.

Key Responsibilities

The selected candidate will:

• Manage clinical study systems and user access.
• Maintain study databases including CTMS, EDC, IWRS, and related platforms.
• Support electronic Trial Master File (eTMF) management.
• Generate study reports and dashboards.
• Track pending actions and coordinate with Clinical Research Associates (CRAs).
• Review investigator packages before regulatory approval.
• Review amended informed consent documents.
• File regulatory documentation into TMF and eTMF.
• Assist study teams during study startup activities.
• Support study communication and coordination.
• Ensure CTMS compliance throughout the study lifecycle.
• Manage investigator payments and invoice processing.
• Perform payment reconciliation during study close-out.
• Support clinical trial documentation and quality review.
• Maintain SOP compliance across assigned studies.
• Participate in continuous process improvement initiatives.
• Track operational metrics and study deliverables.

Investigator Payment Responsibilities

As part of the role, you will:

• Review EDC data and contracts.
• Mark payment milestones in CTMS.
• Generate payment batches.
• Review invoices for quality control.
• Process pass-through expenses.
• Coordinate payment approvals.
• Support financial reconciliation activities.

Required Qualifications

Applicants should possess:

• Bachelor’s Degree in Life Sciences
• OR Nursing
• OR Medical Laboratory Technology
• OR Allied Health Sciences qualification

Equivalent experience may also be considered by Fortrea.

Experience Required

• 3–5 years of Clinical Research experience
• Strong understanding of ICH-GCP guidelines
• Experience with:
  • CTMS
  • eTMF
  • EDC
  • IWRS
  • Clinical documentation
  • Regulatory documentation
  • Study startup
  • Clinical Operations

Desired Skills

Ideal candidates should have:

• Excellent communication skills
• Strong documentation skills
• Attention to detail
• Project coordination ability
• Clinical trial operations knowledge
• Regulatory compliance understanding
• Data review experience
• Study management experience
• Investigator payment management
• Problem-solving mindset
• Team collaboration skills
• Computer proficiency

Why Join Fortrea?

Fortrea is one of the world’s leading Clinical Research Organizations (CROs), providing opportunities to work on global clinical trials across therapeutic areas.

Benefits include:

• Hybrid working model
• Global clinical research exposure
• International project experience
• Career growth opportunities
• Collaborative work culture
• Advanced clinical systems exposure
• Learning and development programs
• Opportunity to work with leading pharmaceutical sponsors

How to Apply

Application Link