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Senior Clinical Data Coordinator (Senior Cdc / Cdc Ii)

Icon Plc
ICON PLC
2-5 years
preferred by company
Chennai, Trivandrum, India
1 May 18, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding

Senior Clinical Data Coordinator (Senior CDC / CDC II)

Location: Chennai, Trivandrum, India
Company: ICON plc
Job Type: Full-Time
Work Mode: Office With Flex (Hybrid)
Department: Clinical Data Management / Clinical Research / Data Operations
Job Reference ID: JR140784
Industry: Clinical Research | CRO | Pharmaceutical | Biotechnology

Job Overview

ICON plc is hiring a Senior Clinical Data Coordinator (Senior CDC / CDC II) for its clinical data management team in India. This opportunity is ideal for experienced professionals with expertise in clinical data management, clinical data cleaning, query management, data reconciliation, clinical trial documentation, ICH-GCP compliance, and cross-functional clinical operations.

As a Senior Clinical Data Coordinator, you will support global clinical trials by managing clinical data workflows, maintaining data quality, resolving discrepancies, and ensuring inspection-ready deliverables. You will collaborate with clinical operations, biostatistics, and study teams while mentoring junior data professionals.

This role is ideal for candidates looking to grow in clinical data management, clinical trial operations, CRO data careers, and healthcare data quality leadership.

Key Responsibilities

Clinical Data Management Operations

  • Create, manage, and maintain clinical data management plans and essential study documentation.
  • Ensure data management deliverables align with project timelines and quality expectations.
  • Support end-to-end clinical trial data workflows.

Data Quality & Data Cleaning

  • Identify, investigate, and resolve clinical data discrepancies.
  • Perform ongoing data cleaning activities to improve accuracy and completeness.
  • Enhance data quality throughout the clinical trial lifecycle.

Clinical Query Management

  • Generate, track, and support resolution of data queries with investigator sites.
  • Ensure timely follow-up for outstanding data issues.
  • Maintain clean and analysis-ready study datasets.

Cross-Functional Collaboration
Work closely with:

  • Clinical Operations
  • Biostatistics
  • Clinical Data Management teams
  • Study management teams
  • Investigator sites
  • Internal stakeholders

Support study-specific data management strategies and execution.

Clinical Documentation & Compliance
Maintain and support:

  • Data management plans
  • Study documentation
  • Filing and archival records
  • Data reconciliation documentation
  • Query tracking records
  • Clinical trial compliance documentation

Ensure inspection readiness and regulatory compliance.

Study Support Activities
Support additional study tasks including:

  • Study filing
  • Documentation archival
  • Data issue escalation
  • Study timeline coordination
  • Data flow management

Mentorship & Team Support

  • Mentor junior Clinical Data Coordinators.
  • Provide guidance on:
    • Data reconciliation
    • Clinical coding
    • Data cleaning
    • Quality processes
    • Best practices in clinical data management

Required Educational Qualification
Candidates must have:

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

Experience Required

  • Experienced candidates only
  • Freshers are not eligible

Required experience includes:

  • Clinical Data Management
  • Clinical trial data operations
  • Data discrepancy management
  • Clinical query handling
  • Pharmaceutical / CRO / biotechnology industry experience

Since this is a Senior CDC / CDC II role, prior hands-on clinical data management experience is mandatory.

Required Skills

  • Clinical Data Management
  • Clinical Data Cleaning
  • Query Management
  • Data Reconciliation
  • Clinical Trial Documentation
  • Data Quality Management
  • Study Data Review
  • Clinical Operations Collaboration
  • Clinical Coding
  • Data Flow Management
  • Regulatory Compliance
  • Clinical Trial Support
  • Mentorship
  • Cross-functional Coordination