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Cdc I

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

 

Clinical Data Coordinator I (CDC I)

Location: Bangalore / Trivandrum / Bengaluru
Job ID: JR137696
Department: Clinical Data Management – ICON Strategic Solutions
Work Model: Office or Home-based


About ICON

ICON plc is a world-leading healthcare intelligence and clinical research organization. We are committed to fostering an inclusive environment that drives innovation and excellence. Join us in our mission to shape the future of clinical development and contribute to improving patient outcomes worldwide.


About the Role

We are seeking a Clinical Data Coordinator I (CDC I) to join our dynamic team. In this role, you will support the clinical data management process by assisting in the design, collection, and analysis of clinical trial data. You’ll help ensure high-quality, reliable data that advances innovative treatments and therapies.


Key Responsibilities

  • Support the Data Management Study Lead in developing:

    • eCRFs (electronic Case Report Forms)

    • Data Validation Specifications

    • Study-Specific Procedures

  • Review clinical and third-party data according to edit specifications and data review plans.

  • Issue clear, accurate, and concise queries to investigational sites for data clarification.

  • Communicate effectively with peers, clinical data scientists, and functional management as required.

  • Perform additional study-related tasks to ensure timelines are met, such as:

    • Filing and archiving study documentation

    • Dispatching queries to investigator sites for resolution


Qualifications & Experience

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

  • Experience: Basic understanding of clinical data management processes within the pharmaceutical or biotechnology industry.

  • Technical Skills:

    • Familiarity with data management software (e.g., Medidata, Oracle RDC, or similar).

    • Knowledge of regulatory guidelines (ICH-GCP) is an advantage.

  • Soft Skills:

    • Strong attention to detail and accuracy.

    • Excellent communication and collaboration skills.

    • Ability to thrive in a fast-paced, team-oriented environment.


What ICON Can Offer You

Our success depends on our people. We are proud to offer a culture that rewards high performance, supports personal growth, and promotes work–life balance.

Benefits include:

  • Competitive salary and annual leave entitlements.

  • Comprehensive health insurance options for you and your family.

  • Retirement planning programs to support your long-term goals.

  • Access to LifeWorks, our Global Employee Assistance Programme—available 24/7 for mental, physical, and emotional well-being support.

  • Life assurance coverage.

  • Additional flexible, country-specific benefits such as:

    • Childcare vouchers

    • Bike purchase schemes

    • Discounted gym memberships

    • Subsidized travel passes

    • Health assessments