Apply for Clinical Data Coordinator I job at Fortrea 2026. Check eligibility, clinical data experience, and application process details now online.
Introduction
The clinical data management field is essential for ensuring the accuracy and integrity of clinical trial results. The Clinical Data Coordinator I Job at Fortrea offers a great opportunity for experienced professionals to work with external clinical data, vendor systems, and global research teams.
This role is ideal for candidates with a background in clinical trials, data handling, and regulatory compliance who want to grow in clinical data management.
Job Overview
| Particulars | Details |
|---|---|
| Job Title | Clinical Data Coordinator I |
| Company Name | Fortrea |
| Location | Bangalore, India |
| Employment Type | Full-Time |
| Department | Clinical Data Management |
| Experience Required | Minimum 3 Years |
| Education | Life Sciences / Health Sciences / IT or related field |
| Salary | As per company norms |
Company Overview
Fortrea is a leading global Contract Research Organization (CRO) that provides clinical development and data solutions to pharmaceutical, biotechnology, and medical device companies.
With a strong focus on innovation and data quality, Fortrea supports clinical trials worldwide and is known for delivering high-quality, reliable research outcomes.
Job Location & Employment Type
This is a full-time position based in Bangalore, India. Candidates may work in a general office or hybrid environment depending on business requirements and should be flexible with shift timings.
Open Positions / Department Details
The role is part of the Clinical Data Management team, focusing on external vendor data handling, validation, and ensuring data quality across clinical studies.
Key Roles & Responsibilities
- Review and maintain external vendor data received from laboratories or central vendors
- Ensure data integrity by verifying correct formats, fields, and patient mapping
- Support development of Data Transfer Agreements (DTA) and specifications
- Review discrepancies generated from edit checks and perform query management
- Validate electronically transmitted data for selected patient samples
- Assist in reviewing external data reports, listings, and status updates
- Coordinate with clinical teams (CTM/CRA) to obtain laboratory normal ranges
- Enter and perform quality checks for laboratory data
- Maintain documentation for data discrepancies and resolutions
- Communicate with vendors and internal teams regarding data transfer issues
- Ensure compliance with SOPs, ICH-GCP guidelines, and global standards
Eligibility Criteria
Education
- Degree in Life Sciences, Health Sciences, Information Technology, or related field
- Certification in allied health professions may also be considered
Experience
- Minimum 3 years of experience in clinical trials, pharma, or biotech industry
- Experience in clinical data management or vendor data handling preferred
Skills Required
- Basic understanding of medical terminology
- Knowledge of clinical data management processes
- Familiarity with ICH-GCP guidelines
- Strong analytical and problem-solving skills
- Good communication and documentation skills
- Ability to handle multiple tasks under pressure
- Proficiency in Microsoft Office tools
- Strong attention to detail and data accuracy
Salary & Benefits
- Salary: As per company norms
- Opportunity to work with a global CRO
- Exposure to international clinical trials and data systems
- Learning and development opportunities
- Collaborative and professional work environment
- Career growth in clinical data management
Selection Process
The hiring process generally includes:
- Resume screening
- Technical interview (clinical data & GCP knowledge)
- HR discussion
- Final selection
How to Apply
Candidates can apply through the official online application portal. Ensure your resume highlights your experience in clinical data management, vendor data handling, and regulatory compliance.
Important Dates
- Last Date to Apply: April 30, 2026
Why Apply for This Job?
The Clinical Data Coordinator I Job at Fortrea offers a strong platform for professionals to build expertise in clinical data management and vendor data processes.
Here’s why this role is valuable:
- Work with a globally recognized CRO
- Gain experience in external vendor data and clinical trials
- Exposure to global regulatory standards
- Opportunity to collaborate with cross-functional teams
- Strong career growth in clinical data and research
This role is ideal for candidates aiming to grow in clinical data management, clinical operations, or regulatory domains.
FAQs
1. What is the eligibility for Clinical Data Coordinator I Job at Fortrea?
Candidates must have a degree in life sciences or related field with at least 3 years of experience.
2. What experience is required for this role?
Experience in clinical trials, data management, or pharma industry is required.
3. What is the job location?
The job is based in Bangalore, India.
4. Is knowledge of ICH-GCP required?
Yes, understanding of ICH-GCP principles is important.
5. What is the last date to apply?
The last date to apply is April 30, 2026.
Conclusion
The Clinical Data Coordinator I Job at Fortrea 2026 is an excellent opportunity for experienced professionals to enhance their skills in clinical data management and vendor data processes. With global exposure, career growth, and a strong work environment, this role is ideal for advancing in the clinical research industry.
Apply early to secure your chance in this growing field.
Disclaimer
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