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Clinical Data Coordinator Ii (Cdc Ii)

Icon Plc
ICON PLC
2-5 years
preferred by company
Bangalore, India
1 May 18, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing

Clinical Data Coordinator II (CDC II)

Location: Bangalore, India / Chennai, India
Company: ICON plc
Job Type: Full-Time
Work Mode: Office with Flex (Hybrid)
Industry: Clinical Research | Clinical Data Management | CRO | Pharmaceutical | Biotechnology
Department: Clinical Data Management
Job Reference ID: JR149422

Job Overview

ICON plc is hiring a Clinical Data Coordinator II (CDC II) for its clinical data management team in Bangalore and Chennai, India. This hybrid opportunity is ideal for professionals with expertise in clinical data management, eCRF maintenance, clinical data reconciliation, query management, clinical database systems, and clinical trial data quality oversight.

The selected candidate will support clinical data management activities across global clinical trials, ensuring high-quality, accurate, and compliant clinical datasets. This role involves collaboration with study leads, clinical data scientists, and cross-functional teams to resolve data issues, manage reconciliations, and maintain study-specific data management deliverables.

This position is ideal for professionals seeking growth in clinical data management, CRO operations, trial data quality, and pharmaceutical clinical research.

Job Responsibilities

Clinical Data Management Support

  • Support end-to-end clinical data management activities for assigned studies.
  • Ensure data quality, consistency, completeness, and regulatory compliance across clinical trial datasets.
  • Deliver clinical data management work to high operational standards.

eCRF Maintenance & Study Documentation

Assist the Data Management Study Lead with:

  • eCRF maintenance
  • Data Validation Specifications (DVS)
  • Study Specific Procedures (SSPs)
  • Study data management documentation
  • Clinical database maintenance support

Ensure study documentation remains current and compliant.

Clinical Data Reconciliation

Manage reconciliation activities including:

  • Clinical data reconciliation
  • Third-party vendor data reconciliation
  • External data consistency review
  • Query-based data review

Ensure alignment with edit specifications and data review plans.

Query Management & Data Issue Resolution

  • Address clinical data-related questions from project stakeholders.
  • Investigate discrepancies and recommend effective resolutions.
  • Identify root causes of recurring data issues.
  • Support systematic issue correction and process improvement.

Clinical Trial Metrics Tracking

Track and communicate study progress metrics to:

  • Clinical Data Scientists
  • Project teams
  • Functional management
  • Data management stakeholders

Provide timely updates on task completion and study performance.

Cross-Functional Collaboration

Collaborate with:

  • Clinical Data Scientists
  • Data Management Study Leads
  • Clinical Operations teams
  • Vendors
  • Project teams
  • Cross-functional stakeholders

Support smooth clinical trial execution and timely data delivery.

Regulatory Compliance & Quality Oversight

Ensure adherence to:

  • ICH-GCP guidelines
  • Clinical data management standards
  • Internal SOPs
  • Quality procedures
  • Sponsor/client requirements

Maintain audit-ready data management practices.

Educational Qualification

Candidates must have:

  • Bachelor’s Degree in:
    • Life Sciences
    • Pharmacy
    • Healthcare
    • Biotechnology
    • Biomedical Sciences
    • Related relevant discipline

Experience Requirements

  • Minimum 2–5 years of relevant clinical data management experience
  • Freshers are not eligible

Preferred experience in:

  • Pharmaceutical industry
  • Biotechnology industry
  • CRO clinical data management
  • Global clinical trial support

Mandatory exposure to:

  • Clinical data reconciliation
  • Query management
  • eCRF maintenance
  • Clinical data review