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Cdc Ii (Clinical Data Coordinator Ii)

ICON PLC
1-3 years
INR 6 LPA – 11 LPA
Bangalore, Chennai, Trivandrum, India
1 June 29, 2026
Job Description
Job Type: Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

CDC II (Clinical Data Coordinator II)

Company: ICON plc
Location: Bangalore / Chennai / Trivandrum, India
Department: Clinical Data Management
Job Type: Full-Time
Work Mode: Office or Home (Hybrid)

JOB OVERVIEW

The Clinical Data Coordinator II (CDC II) is responsible for supporting clinical data management activities for global clinical trials by ensuring the quality, accuracy, and integrity of clinical data. The role involves maintaining electronic Case Report Forms (eCRFs), managing data reconciliation, resolving data discrepancies, tracking study metrics, supporting clinical data review activities, and collaborating with cross-functional teams to ensure compliance with regulatory requirements and study timelines.

KEY RESPONSIBILITIES

Clinical Data Management

  • Support the Data Management Study Lead in clinical data management activities.

  • Maintain electronic Case Report Forms (eCRFs).

  • Assist in preparing and maintaining Data Validation Specifications (DVS).

  • Develop and update Study Specific Procedures (SSPs).

  • Ensure clinical data quality throughout the study lifecycle.

Data Review & Reconciliation

  • Perform reconciliation of clinical and third-party data.

  • Review data according to edit specifications and Data Review Plans.

  • Identify, investigate, and resolve data discrepancies.

  • Validate data consistency across multiple data sources.

  • Ensure timely completion of reconciliation activities.

Data Quality Management

  • Review clinical data for completeness, consistency, and accuracy.

  • Investigate data queries and recommend appropriate resolutions.

  • Perform root cause analysis for recurring data issues.

  • Support implementation of corrective and preventive actions.

  • Maintain high standards of data integrity and quality.

Study Tracking & Reporting

  • Track study progress and task completion metrics.

  • Communicate study status to Clinical Data Scientists and project teams.

  • Prepare study progress reports and status updates.

  • Monitor assigned deliverables to ensure adherence to timelines.

  • Support study milestone tracking and reporting.

Cross-Functional Collaboration

  • Collaborate with Clinical Data Scientists, Clinical Operations, Biostatistics, and Project Management teams.

  • Respond to data-related queries from internal stakeholders.

  • Support issue resolution across functional teams.

  • Participate in project meetings and data review discussions.

  • Contribute to continuous process improvements.

Regulatory Compliance

  • Ensure compliance with ICH-GCP guidelines and applicable regulatory standards.

  • Follow company SOPs, work instructions, and quality procedures.

  • Maintain audit-ready study documentation.

  • Support inspection readiness and quality compliance activities.

  • Ensure confidentiality and integrity of clinical trial data.

EDUCATIONAL QUALIFICATIONS

Required

Bachelor's Degree in:

  • Life Sciences

  • Pharmacy

  • Biotechnology

  • Biomedical Sciences

  • Nursing

  • Clinical Research

  • Healthcare

  • Or a related discipline

Preferred

  • Master's Degree in Life Sciences, Clinical Research, Pharmacy, Biotechnology, or Healthcare.

EXPERIENCE REQUIREMENTS

Required

  • Experience in Clinical Data Management within the pharmaceutical, biotechnology, CRO, or clinical research industry.

  • Knowledge of clinical data management processes and workflows.

  • Familiarity with Electronic Data Capture (EDC) systems.

Preferred

  • Experience with Medidata Rave, Oracle RDC, or similar EDC platforms.

  • Experience with data reconciliation and query management.

  • Knowledge of ICH-GCP and clinical trial regulations.

  • Experience supporting global clinical studies.