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Sr. Centralized Study Coordinator

Fortrea
2-3 years
Not Disclosed
Bangalore, India
2 May 21, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs

Sr. Centralized Study Coordinator

Company: Fortrea
Job Title: Sr. Centralized Study Coordinator
Job ID: 261436
Location: Bengaluru, Karnataka
Job Category: Clinical Operations / Clinical Trial Management Support
Employment Type: Full-time


Job Summary

Fortrea is hiring a Sr. Centralized Study Coordinator to support clinical trial operations through study coordination, clinical systems management, investigator payment processing, document management, CTMS compliance, and study support activities. This role acts as a centralized operational support function for global clinical studies.


Key Responsibilities

Clinical Systems & Study Support

  • Manage access for clinical systems and study tools.

  • Maintain study platforms including:

    • CTMS

    • IWRS

    • EDC

    • Other clinical systems

  • Perform system setup for newly awarded studies.

  • Support study teams in:

    • Data review activities

    • eTMF document management

    • Study support operations

    • Report generation

  • Follow up with CRAs for pending action items and issue resolution.

  • Assist leads with study-specific data review tasks.

  • Manage project communications and operational coordination.

  • Support site startup and study activation activities.


Investigator Payment Management

  • Review:

    • EDC records

    • Contracts

    • Payment eligibility in CTMS

  • Mark line items:

    • Ready to Pay

    • Screen Failure

  • Coordinate invoice generation and payment batch creation.

  • Perform invoice QC and prepare GIA documentation.

  • Coordinate approvals with:

    • CTL

    • Project Managers

  • Process:

    • Out-of-pocket expenses

    • Pass-through invoices

  • Perform payment reconciliation during study closeout.


Documentation & Compliance

  • Maintain project and technical documentation.

  • Support document lifecycle management including:

    • Template creation

    • Collection

    • Review

    • Processing

    • Tracking

    • eTMF filing

  • Assist in investigator submission package preparation.

  • Ensure CTMS compliance and process adherence.

  • Track metrics and report according to timelines.

  • Support implementation of revised SOPs and procedures.

  • Ensure quality checks and timely issue escalation.


Required Qualifications

  • University / College Degree (Life Sciences preferred)

OR

  • Allied Health Certification:

    • Nursing

    • Medical Technology

    • Laboratory Technology

Equivalent relevant experience may be considered.


Required Experience

  • 2–3 years of clinical research experience

  • Strong knowledge of:

    • ICH-GCP guidelines

    • Clinical trial processes

    • Clinical operations support

Experience in:

  • Study coordination

  • Clinical systems

  • Documentation management

  • Investigator payment workflows