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Cdc I

1.5 years
Not Disclosed
10 Nov. 12, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Clinical Data Coordinator I (CDC I)

Locations:

Bangalore | Chennai | Trivandrum | Bengaluru

Job Requisition ID: JR136881

Department:

Clinical Data Management – ICON Strategic Solutions

Job Type:

  • Employment Type: Full-time

  • Work Arrangement: Office-based

  • Functional Area: Clinical Data Management

Experience Level:

  • Approximately 1.5 years of relevant experience in Clinical Data Management activities


About the Role

ICON plc is a world-leading healthcare intelligence and clinical research organization committed to advancing the future of clinical development. We are seeking a Clinical Data Coordinator I (CDC I) to join our diverse and innovative team.

As a Clinical Data Coordinator I, you will support data management activities across clinical studies, ensuring the integrity, accuracy, and quality of clinical trial data that drive groundbreaking research and drug development.


Key Responsibilities

  • Support the Data Management Study Lead in developing eCRFs, Data Validation Specifications, and Study-Specific Procedures.

  • Review clinical and third-party data based on edit check specifications and data review plans.

  • Generate and issue clear, concise, and accurate data queries to investigational sites.

  • Collaborate effectively with team members, Clinical Data Scientists, and functional management to meet study timelines.

  • Perform project-related activities such as documentation, TMF filing, and dispatching site queries for resolution.

  • Contribute to the quality and compliance of all data management deliverables in accordance with ICH-GCP and company SOPs.


Your Profile

  • Education: Bachelor’s degree in Life Sciences, Healthcare, or a related discipline.

  • Experience: Minimum 1.5 years of experience in Clinical Data Management, including:

    • Data review and query management

    • Database design and testing

    • TMF documentation

    • Implementation of data tools using EDC systems (e.g., Medidata, Oracle RDC).

  • Skills:

    • Strong attention to detail and accuracy

    • Proficiency in data management software and systems

    • Excellent written and verbal communication skills

    • Ability to work collaboratively in cross-functional environments

  • Preferred Knowledge: Understanding of regulatory standards (ICH-GCP) and data integrity principles.


What ICON Can Offer You

ICON’s success is driven by the excellence of its people. We foster a diverse, high-performance culture focused on innovation, collaboration, and well-being.

Benefits include:

  • Competitive salary and performance-based rewards

  • Various annual leave entitlements

  • Comprehensive health insurance plans for you and your family

  • Competitive retirement planning options

  • Access to Global Employee Assistance Programme (LifeWorks) for 24/7 professional and personal support

  • Life assurance

  • Flexible, country-specific benefits such as childcare vouchers, gym memberships, health assessments, and travel subsidies