Clinical Data Coordinator I – Clinical Data Management Jobs in Bangalore | Fortrea Careers 2026
Location: Bangalore
Job Type: Full-Time
Company: Fortrea
Department: Clinical Data Management (CDM)
Experience Required: FRESHERS or Minimum 3 Years
Industry: Pharmaceutical, Biotechnology, Clinical Research, Medical Devices, Diagnostics
Application Deadline: May 8, 2026
About the Role
Fortrea is hiring experienced professionals for the position of Clinical Data Coordinator I in Bangalore. This opportunity is ideal for candidates looking to build a long-term career in Clinical Data Management (CDM), Clinical Research Operations, Vendor Data Management, and Electronic Clinical Data Review within the global pharmaceutical and biotechnology industry.
The selected candidate will support external vendor and laboratory data management activities while ensuring compliance with ICH-GCP guidelines, protocol specifications, data integrity standards, and global SOPs across clinical trials.
This role offers excellent exposure to clinical trial data validation, vendor data reconciliation, query management, laboratory data review, and electronic data transfer processes in an international CRO environment.
Key Responsibilities
External Vendor Data Review & Management
Review, maintain, and update electronic external vendor and laboratory data.
Ensure vendor data contains all protocol-defined parameters and populates accurately into study databases.
Verify correct formatting, mapping, and patient-level data integration.
Clinical Data Validation & Quality Control
Support review and validation of electronically transmitted external data.
Perform quality checks for laboratory normal ranges and ensure correct attachment to patient records.
Review external data edit checks, listings, and status reports.
Query Management & Discrepancy Resolution
Review study-specific discrepancies generated through edit checks.
Coordinate query management activities for external clinical data issues.
Research and resolve inconsistent laboratory reference range information.
Clinical Trial Coordination Support
Interact with Clinical Trial Managers (CTM), Clinical Research Associates (CRA), and internal study teams.
Support preparation of Data Transfer Agreements (DTA) and Data Transfer Specifications (DTS).
Assist in communication with vendors regarding transfer issues, validation concerns, and data discrepancies.
Compliance & Documentation
Maintain documentation according to global SOPs and regulatory standards.
Ensure confidentiality, accuracy, and integrity of clinical trial data throughout the study lifecycle.
Eligibility Criteria
Educational Qualification
Candidates must possess:
A university or college degree in:
Life Sciences
Health Sciences
Information Technology
Clinical Research
Pharmacy
Biotechnology
Related healthcare disciplines
OR
Certification in allied health professions from a recognized institution.
Relevant industry experience may also be considered in place of formal educational qualifications.
Experience Required
Minimum 3 years of experience in:
Clinical Data Management
Pharmaceutical Industry
Biotechnology Industry
Clinical Trials
Medical Devices
Diagnostics
Freshers are not eligible for this position.
Required Skills
Technical Skills
Understanding of Clinical Data Management workflows
Knowledge of ICH-GCP principles
Familiarity with vendor data transfer processes
Experience with query management and data reconciliation
Strong technical aptitude
Proficiency in Microsoft Office Suite
Soft Skills
Strong organizational and planning skills
Excellent written and verbal communication skills
Critical-thinking and analytical abilities
Ability to handle multiple priorities under tight timelines
Professional collaboration with sponsors and internal stakeholders
Additional Preferred Skills
Basic understanding of medical terminology
Experience working with laboratory data
Ability to work in flexible shifts as per business requirements
Work Environment
General office or remote working environment
Long-duration computer-based work
Frequent priority changes and multitasking requirements
Collaborative global clinical research setting
Why Join Fortrea?
Working with Fortrea provides professionals with exposure to:
Global clinical trials
Advanced Clinical Data Management systems
International pharmaceutical sponsors
Regulatory-compliant clinical operations
Career growth opportunities in CRO and life sciences sectors
This role is highly suitable for professionals aiming to strengthen their careers in:
Clinical Data Management (CDM)
Clinical Research
Pharmacovigilance
Biostatistics Support
Trial Data Operations
Regulatory Clinical Documentation
How to Apply
Interested and eligible candidates can apply directly through the official careers portal of Fortrea before the application deadline.
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