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Clinical Data Coordinator I (Cdc I)

Icon
ICON
0-2 years
Not Disclosed
Bangalore, Trivandrum, India
2 May 6, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Data Coordinator I (CDC I)

Location: Bangalore, India / Trivandrum, India
Work Mode: Office or Home (Hybrid/Flexible)
Job Type: Full-Time
Experience Required: Freshers Eligible | 0–2 Years of Experience Preferred
Industry: Clinical Research / Clinical Data Management / Pharmaceutical


Job Overview

We are seeking a detail-oriented and motivated Clinical Data Coordinator I (CDC I) to support clinical data management activities within global clinical research projects. The selected candidate will assist in clinical trial data review, query management, eCRF development support, and study documentation processes while ensuring data quality and compliance with industry standards.

This role is ideal for freshers and early-career professionals interested in building a career in clinical data management, clinical research, and healthcare analytics within pharmaceutical, biotechnology, or CRO environments.


Key Responsibilities

Clinical Data Management Support

  • Assist the Data Management Study Lead in:
    • eCRF development
    • Data Validation Specifications
    • Study-specific procedures
    • Clinical data workflows
  • Support accurate and timely clinical data processing activities.

Clinical Data Review & Query Management

  • Review:
    • Clinical trial data
    • Third-party data
    • Patient records
      based on predefined edit checks and data review plans.
  • Generate and issue:
    • Clear
    • Accurate
    • Concise data queries
      to investigational sites for resolution.
  • Ensure high-quality data collection and maintenance throughout the study lifecycle.

Documentation & Study Coordination

  • Support project-related activities including:
    • Filing and archiving study documents
    • Query tracking
    • Study documentation management
    • Data reconciliation support
  • Assist in meeting study timelines and project deliverables.

Cross-Functional Collaboration

  • Communicate effectively with:
    • Clinical Data Scientists
    • Functional managers
    • Clinical operations teams
    • Cross-functional stakeholders
  • Participate in team discussions and support operational coordination activities.

Regulatory Compliance & Quality Standards

  • Follow industry standards and best practices related to:
    • Clinical data management
    • ICH-GCP guidelines
    • Regulatory compliance
    • Data integrity
  • Ensure clinical data activities meet quality and compliance expectations.

Required Qualifications

Educational Qualifications

Required Qualification:

  • Bachelor’s Degree in:
    • Life Sciences
    • Pharmacy
    • Biotechnology
    • Clinical Research
    • Healthcare
    • Nursing
    • Biochemistry
    • Or related scientific disciplines

Preferred Qualifications

  • Certifications in:
    • Clinical Research
    • Clinical Data Management
    • Pharmacovigilance
    • Healthcare Analytics
  • Basic knowledge of:
    • Clinical trial processes
    • Data management systems
    • Regulatory guidelines

Experience Requirements

Freshers Eligibility

  • Freshers are eligible to apply.

Preferred Experience

  • 0–2 years of experience in:
    • Clinical Data Management
    • Clinical Research
    • Healthcare Operations
    • CRO or Pharmaceutical environments

Internship experience in clinical research or healthcare data management will be an added advantage.