Apply for Clinical Data Coordinator I job at Fortrea 2026. Check eligibility, experience requirements, and clinical data role details online now today.
Introduction
Clinical data management is a vital component of clinical trials, ensuring accuracy, consistency, and regulatory compliance. The Clinical Data Coordinator I Job at Fortrea offers a strong opportunity for experienced professionals to work with external vendor data and contribute to high-quality clinical research outcomes.
This role is ideal for candidates with prior experience in clinical trials, data validation, and regulatory standards who want to grow in the clinical data management domain.
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 global Contract Research Organization (CRO) that provides clinical development, data management, and regulatory services to pharmaceutical, biotechnology, and medical device companies.
Fortrea is known for its focus on data integrity, innovation, and delivering reliable clinical trial outcomes across global markets.
Job Location & Employment Type
This is a full-time position based in Bangalore, India. Candidates should be comfortable working in flexible shifts and handling multiple priorities in a dynamic environment.
Open Positions / Department Details
The role is part of the Clinical Data Management team, focusing on handling external vendor data, validation processes, and ensuring compliance with clinical trial protocols.
Key Roles & Responsibilities
- Review, maintain, and update external vendor data from laboratories and vendors
- Ensure data accuracy, completeness, and correct mapping to patient records
- Support preparation of Data Transfer Agreements (DTA) and specifications
- Identify and resolve data discrepancies through query management
- Perform validation checks on electronically transmitted clinical data
- Assist in reviewing data listings, reports, and edit checks
- Coordinate with clinical teams to obtain laboratory normal ranges
- Perform quality control (QC) checks on lab data entries
- Maintain proper documentation for data discrepancies and resolutions
- Communicate with vendors and internal teams regarding data issues
- Ensure compliance with SOPs, ICH-GCP guidelines, and regulatory standards
Eligibility Criteria
Education
- Degree in Life Sciences, Health Sciences, Information Technology, or related field
- Equivalent experience or certification 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 principles
- Strong analytical and problem-solving skills
- Good communication and documentation abilities
- Proficiency in Microsoft Office tools
- Ability to handle multiple tasks efficiently
- High attention to detail and data accuracy
Salary & Benefits
- Salary: As per company norms
- Opportunity to work with a global CRO
- Exposure to international clinical trial data systems
- Learning and development opportunities
- Professional and collaborative 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 handling, vendor data, 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 is a strong opportunity for professionals to enhance their expertise in clinical data management and vendor data processes.
Key advantages include:
- Work with a globally recognized CRO
- Gain experience in clinical data validation and management
- Exposure to global regulatory standards
- Opportunity to collaborate with cross-functional teams
- Strong career growth in clinical research and data management
This role is ideal for candidates aiming to build long-term careers 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 relevant degree with at least 3 years of experience in clinical trials or data management.
2. What experience is required for this role?
Experience in pharma, biotech, or clinical trial data handling 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 provides an excellent platform for experienced professionals to grow in clinical data management. With global exposure, skill development, and strong career prospects, this role is ideal for advancing in the clinical research field.
Apply early to secure this opportunity.
Disclaimer
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