Central Monitor Assistant
Company
Fortrea – A global clinical research organization providing clinical trial management, data operations, and regulatory support services to ensure efficient and compliant study execution.
Job Details
Job Title: Central Monitor Assistant
Job Requisition ID: 262504
Employment Type: Full-time
Location: Bangalore, India
Application Deadline: June 30, 2026
About the Role
The Central Monitor Assistant supports clinical study management activities by assisting with data review, system management, investigator payments, and study documentation.
This role ensures smooth study execution by maintaining clinical systems, supporting data quality checks, and coordinating with study teams across multiple operational areas.
Key Responsibilities
1. Clinical Systems & Access Management
Manage access to clinical systems such as:
CTMS
IWRS
EDC
Support system setup for newly awarded studies.
Ensure proper user access control and system compliance.
2. Study Database & Documentation Support
Maintain study databases and trackers.
Support eTMF (electronic Trial Master File) management activities.
Assist in document collection, review, tracking, and filing.
3. Data Review & Issue Management
Support clinical data review activities.
Follow up with CRAs to resolve outstanding issues and action items.
Assist study leads with data review-related tasks.
4. Reporting & Metrics
Generate study-specific reports.
Track and report study metrics as required.
Assist in CTMS compliance management.
5. Investigator Payments
Review EDC, contract data, and mark items as:
“Ready to Pay”
“Screen Failure”
Assist in invoice processing, reconciliation, and payment tracking.
Coordinate with study teams for approvals and payment execution.
6. Study Support Activities
Assist in study startup and site activation tasks.
Support preparation of investigator submission packages.
Assist in investigator payment processing and reconciliation.
Support contract management activities for assigned studies.
7. Communication & Coordination
Manage project communications and follow-ups.
Coordinate with CTLs, PMs, and study teams.
Ensure timely escalation of issues and resolution.
8. Quality & Compliance
Follow SOPs, work instructions, and GCP guidelines.
Ensure high-quality and timely completion of tasks.
Assist in audit readiness and documentation accuracy.
9. Process Improvement
Support implementation of revised processes.
Assist in improving workflow efficiency and documentation practices.
Required Qualifications
Education
University/College degree (Life Sciences preferred), or
Allied health certification (e.g., Nursing, Lab Technology)
Experience
2–3 years of experience in clinical research.
Strong understanding of:
ICH-GCP guidelines
Clinical trial operations
Skills & Competencies
Strong organizational and multitasking abilities.
Excellent attention to detail.
Strong communication skills (written and verbal).
Ability to work effectively in a team environment.
Proficiency with clinical systems and computer tools.
Ability to maintain high-quality output under deadlines.
Additional Requirements
Fluent in English.
Ability to manage administrative and technical study support tasks.
Willingness to follow structured processes and compliance standards.
Inclusion & Accessibility
Fortrea is committed to equal opportunity employment and fostering an inclusive workplace.
Reasonable accommodations are available during the recruitment process upon request.
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Remote, India | Siliguri |Illinois :
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Canada |Quebec :
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Japan | Saitama |Tokyo :
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Oulu |Southwest Finland (Varsinais-Suomi) :
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