Fortrea Hiring Clinical Data Coordinator I
- Fortrea Hiring Clinical Data Coordinator I in Bangalore | Apply Now for Clinical Research Roles
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Skills Required:
- Experience:
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- What kind of work will I be doing?
- What industry experience is preferred?
- Is knowledge of ICH-GCP required?
- What are the growth opportunities?
Fortrea Hiring Clinical Data Coordinator I in Bangalore | Apply Now for Clinical Research Roles
Fortrea is inviting applications for the role of Clinical Data Coordinator I at its Bangalore location. This opportunity is ideal for candidates with experience in clinical data management, clinical trials, and healthcare data analysis who are looking to grow in a global CRO environment. The company is hiring for full-time positions in the clinical data management department, offering a strong platform to work on global clinical research projects and regulated data systems.
This role is not a fresher role. Candidates with relevant experience in clinical research, biotechnology, pharmaceutical, or medical device industries will find this position aligned with long-term career growth in clinical data management and regulatory-compliant environments.
Company Overview
Fortrea is a leading global contract research organization (CRO) that supports pharmaceutical, biotechnology, and medical device companies in conducting clinical trials and advancing healthcare innovation. Known for its strong focus on data integrity, regulatory compliance, and patient safety, Fortrea delivers high-quality clinical development and data management solutions across global markets.
Working at Fortrea provides exposure to international clinical trials, advanced data management systems, and industry-leading practices aligned with ICH-GCP guidelines. The company plays a critical role in accelerating drug development and ensuring accurate, reliable clinical data for regulatory submissions.
Job Role & Responsibilities
As a Clinical Data Coordinator I, you will be responsible for managing and validating external clinical data received from vendors and laboratories. This role focuses heavily on clinical data review, query management, and ensuring data consistency across clinical trial databases.
Key responsibilities include:
- Review and validate external vendor data to ensure accuracy and protocol compliance
- Ensure data is correctly formatted and mapped to appropriate patient records
- Support development of Data Transfer Agreements (DTA) and Data Transfer Specifications (DTS)
- Identify discrepancies through edit checks and perform query management to resolve issues
- Assist in validation and quality checks of electronically transmitted clinical data
- Review external data listings, reports, and edit checks
- Collaborate with clinical teams (CTM/CRA) to collect and verify laboratory normal ranges
- Perform quality control checks on local laboratory data entries
- Maintain documentation aligned with regulatory and audit requirements
- Communicate with vendors and internal teams regarding data issues and resolution
This role directly contributes to maintaining high-quality clinical trial data, which is essential for regulatory submissions, drug safety evaluation, and successful clinical research outcomes.
Eligibility / Qualifications
Candidates must meet the following educational requirements:
BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Pharmacy, Clinical Research, Health Sciences, B.Tech Biotechnology, B.Tech Bioinformatics, Information Technology, Allied Health Sciences
Skills Required:
- Strong understanding of clinical data management and clinical trial processes
- Knowledge of ICH-GCP guidelines and regulatory compliance
- Familiarity with medical terminology and clinical databases
- Strong analytical and problem-solving skills
- Ability to manage multiple tasks under tight timelines
- Proficiency in Microsoft Office tools (Excel, Word, etc.)
- Strong communication and documentation skills
Experience:
- Minimum 3 years of experience in clinical research, CRO, pharmaceutical, or biotechnology industry
Location & Salary
- Location: Bangalore
- Salary: Competitive salary package as per CRO industry standards
Application Process
Interested candidates can apply through the official Fortrea careers portal using the link below:
Apply Here: https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Bangalore/External-Data-Reviewer_26721
Candidates are encouraged to apply before the deadline as applications are reviewed on a rolling basis.
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
No, this role requires a minimum of 3 years of experience in clinical data management or related fields.
What kind of work will I be doing?
You will be handling clinical trial data, validating external vendor data, resolving discrepancies, and ensuring regulatory compliance.
What industry experience is preferred?
Experience in pharmaceutical, biotechnology, CRO, or medical device industries is preferred.
Is knowledge of ICH-GCP required?
Yes, a basic understanding of ICH-GCP guidelines is important for this role.
What are the growth opportunities?
This role can lead to positions such as Clinical Data Manager, Lead Data Manager, or roles in regulatory and clinical operations.
| Category | Details |
|---|---|
| Company | Fortrea |
| Vacancies | Clinical Data Coordinator I |
| Required Education | BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Pharmacy, Clinical Research, Health Sciences, B.Tech Biotechnology, B.Tech Bioinformatics, Information Technology, Allied Health Sciences |
| Experience | Minimum 3 Years |
To apply for this job please visit fortrea.wd1.myworkdayjobs.com.
