Central Monitoring Specialist job at Fortrea Bangalore. Check eligibility, experience, responsibilities, last date April 30, and apply online today now.
Introduction
If you have experience in clinical research and want to move into advanced monitoring and risk-based trial management, this opportunity is highly valuable. The Central Monitoring Specialist Job at Fortrea focuses on data-driven clinical trial monitoring, risk assessment, and analytics.
This role is ideal for professionals with clinical operations, data management, or monitoring experience who want to work on global trials using advanced informatics platforms.
Job Overview
| Details | Information |
|---|---|
| Job Title | Central Monitoring Specialist |
| Company Name | Fortrea |
| Location | Bangalore, India |
| Employment Type | Full-time |
| Department | Clinical Operations / Central Monitoring |
| Experience Required | 3–5 Years |
| Education | Life Sciences (Preferred) |
| Salary | As per company standards |
Company Overview
Fortrea is a globally recognized CRO providing clinical development and data-driven solutions to pharmaceutical and biotech companies. The organization is known for its expertise in clinical operations, risk-based monitoring, and advanced analytics in clinical trials.
Working at Fortrea offers exposure to global studies, innovative monitoring strategies, and cutting-edge clinical data platforms.
Job Location & Employment Type
- Location: Bangalore, India
- Employment Type: Full-time
- Work Mode: Office/Hybrid (as per business requirements)
Open Positions / Department Details
- Role: Central Monitoring Specialist
- Department: Clinical Operations / Risk-Based Monitoring
- Focus on centralized monitoring, risk assessment, and clinical analytics.
Key Roles & Responsibilities
As a Central Monitoring Specialist, your responsibilities will include:
Central Monitoring & Risk Assessment
- Performing centralized monitoring activities across multiple studies
- Reviewing site, subject, and study-level data
- Identifying risks and recommending mitigation strategies
Data Review & Analytics
- Analyzing risk indicators and study data from various systems (EDC, lab data, etc.)
- Conducting subject-level and site-level data reviews
- Supporting data-driven decision-making
Study Coordination & Reporting
- Preparing and reviewing risk reports and study status reports
- Organizing study risk assessment meetings
- Tracking and resolving site issues and queries
System & Tool Management
- Supporting informatics platforms and visualization tools
- Writing and executing User Acceptance Testing (UAT) scripts
- Managing data in systems like eTMF or Veeva Vault
Process Improvement & Collaboration
- Collaborating with project teams and stakeholders
- Suggesting process improvements and system enhancements
- Supporting study scope and risk profile updates
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences (preferred)
- Postgraduate degree is an added advantage
Experience
- 3–5 years of experience in:
- Clinical research
- Clinical monitoring
- Data management
- Project management
Skills Required
- Strong analytical and problem-solving skills
- Knowledge of clinical trial processes and risk-based monitoring
- Good understanding of ICH-GCP guidelines
- Excellent planning and organizational skills
- Ability to work with data systems and informatics platforms
- Communication and stakeholder management skills
Salary & Benefits
- Salary: As per company standards
- Opportunity to work on global clinical trials
- Exposure to advanced risk-based monitoring strategies
- Career growth in clinical operations and analytics
- Learning opportunities in informatics and data science
- Collaborative work environment
Selection Process
The hiring process typically includes:
- Resume screening
- Technical interview (clinical & data concepts)
- HR discussion
- Final selection
How to Apply
- Candidates should apply through the official Fortrea careers portal.
- Ensure your CV highlights relevant clinical research and monitoring experience.
Important Dates
- Last Date to Apply: April 30, 2026
Why Apply for This Job?
The Central Monitoring Specialist Job at Fortrea is an advanced role for professionals looking to grow in clinical research and data-driven trial management.
Here’s why this role is important:
- Work on global, multi-site clinical trials
- Gain expertise in risk-based monitoring and analytics
- Exposure to modern clinical data platforms
- Opportunity to grow into:
- Clinical Project Manager
- Risk-Based Monitoring Lead
- Clinical Data Scientist
- Clinical Operations Manager
FAQs
1. Who can apply for this job?
Candidates with Life Sciences degrees and clinical research experience can apply.
2. What is the required experience?
3–5 years of experience in clinical research or related roles is required.
3. What is the last date to apply?
The last date to apply is April 30, 2026.
4. What skills are required?
Analytical skills, clinical trial knowledge, data handling, and communication skills are essential.
5. How can I apply?
You can apply through the official Fortrea careers website.
Conclusion
The Central Monitoring Specialist Job at Fortrea is a great opportunity for experienced clinical research professionals to move into advanced monitoring and analytics roles. With exposure to global trials and innovative systems, this role offers strong career growth potential.
If you have the required experience and want to advance in clinical operations, apply before the deadline.
Disclaimer
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