Location: Bangalore, India
Job Type: Full-Time
Company: Fortrea
Application Deadline: May 8, 2026
Experience Required: Minimum 3 Years Experience (Freshers Not Eligible)
About the Company
Fortrea is a leading global Contract Research Organization (CRO) providing clinical development, patient access, and technology-driven solutions to pharmaceutical, biotechnology, and medical device companies worldwide. The organization is known for delivering advanced clinical trial solutions and maintaining high-quality standards across global healthcare research projects.
Job Overview
Fortrea is hiring for the position of Clinical Data Coordinator I in Bangalore. This role is ideal for experienced professionals in Clinical Data Management (CDM), Clinical Research, Biotechnology, Life Sciences, and Healthcare Analytics who possess strong technical and analytical capabilities in external vendor data management and clinical trial data integrity.
The selected candidate will support external laboratory and vendor data review activities while ensuring compliance with ICH-GCP guidelines, protocol specifications, and global clinical data management standards.
Key Responsibilities
Review, maintain, and update external vendor and laboratory data received during clinical trials
Ensure protocol-specific parameters are correctly captured and populated within clinical databases
Support the development of Data Transfer Agreements (DTA) and Data Transfer Specifications for external vendor data
Review and resolve external data discrepancies generated through study-specific edit checks
Assist in validation review of electronically transmitted clinical trial data
Perform quality control and review of external data listings, reports, and edit checks
Coordinate with Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) to obtain and verify local laboratory normal ranges
Maintain accurate documentation and ensure proper attachment of laboratory normal ranges to patient records
Communicate data transfer, validation, and data quality issues with vendors and internal stakeholders
Ensure adherence to SOPs, ICH-GCP principles, and clinical data integrity standards
Support multiple ongoing clinical projects while maintaining confidentiality and compliance
Educational Qualifications
Bachelor’s or Master’s degree in:
Life Sciences
Pharmacy
Biotechnology
Health Sciences
Information Technology
Related Healthcare or Scientific disciplines
OR
Certification in allied health professions from a recognized institution
Equivalent industry experience may also be considered.
Required Experience & Skills
Experience Required
Minimum 3 years of experience in:
Clinical Data Management
Pharmaceutical Industry
Biotechnology Industry
Clinical Trials
Medical Device or Diagnostics Industry
Preferred Skills
Basic understanding of medical terminology
Knowledge of ICH-GCP guidelines and clinical trial workflows
Strong analytical, organizational, and critical-thinking abilities
Excellent written and verbal communication skills in English
Ability to manage multiple priorities under tight deadlines
Proficiency in Microsoft Office Suite and clinical data systems
Strong technical aptitude and problem-solving skills
Ability to maintain confidentiality of sensitive clinical trial data
Work Environment & Shift Requirements
Office-based or remote working environment
Requires extended computer-based work
Flexible shift availability may be required based on business needs
Ability to work effectively in fast-paced clinical research environments
Who Should Apply?
This role is highly suitable for experienced professionals looking to build long-term careers in:
Clinical Data Management (CDM)
Clinical Research
Pharmacovigilance
Healthcare Analytics
CRO Operations
Biotech & Pharmaceutical Research
Freshers are not eligible for this position due to the required industry experience.
Why This Opportunity Matters
With the rapid growth of global clinical trials and healthcare data management, experienced Clinical Data Management professionals are in high demand across top CROs and pharmaceutical companies. This role offers exposure to global clinical trial operations, vendor data handling, regulatory compliance, and cross-functional collaboration in one of the world’s fastest-growing healthcare sectors.
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