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Cdc Ii

Icon Plc
ICON PLC
10 Jan. 22, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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 II (CDC II)
Job ID / Requisition Number: JR141730
Location: Chennai, Trivandrum, Bangalore, India
Work Type: Office with Flexibility
Employment Type: Full-time
Application Deadline: January 23, 2026


About ICON

ICON plc is a global leader in healthcare intelligence and clinical research, dedicated to advancing patient care through innovation and scientific excellence. Our inclusive culture fosters collaboration, learning, and professional growth, enabling teams to drive transformative clinical development across the pharmaceutical and biotechnology industries.


Role Overview

The Clinical Data Coordinator II (CDC II) plays a critical role in clinical trial data management, ensuring accuracy, integrity, and compliance of study data. You will support data collection, reconciliation, validation, and reporting while collaborating with cross-functional teams to optimize clinical trial outcomes.


Key Responsibilities

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

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

  • Track, monitor, and report study and task metrics to the project team, clinical data scientists, and functional management.

  • Address data queries, identify root causes of data issues, and recommend corrective actions.

  • Support overall data quality, compliance, and adherence to study timelines.


Qualifications & Experience

Required:

  • Bachelor’s degree in Life Sciences, Healthcare, or a relevant field.

  • Minimum 5 years of experience in clinical data management within the pharmaceutical or biotechnology industry.

  • Intermediate knowledge of clinical data management processes and systems (e.g., Medidata Rave, Oracle RDC, or equivalent).

  • Strong attention to detail, analytical skills, and the ability to work effectively in a fast-paced environment.

  • Excellent communication and collaboration skills for cross-functional engagement.

Preferred:

  • Familiarity with regulatory guidelines and standards (e.g., ICH-GCP).


Why ICON?

  • Join a global, inclusive, and supportive workplace culture that values diversity and belonging.

  • Competitive salary and benefits including health insurance, retirement planning, life assurance, and flexible country-specific options such as childcare vouchers, gym memberships, and travel allowances.

  • Professional growth opportunities and access to a global network of clinical research experts.

  • Commitment to inclusion, accessibility, and reasonable accommodations for candidates with disabilities or medical conditions.

At ICON, your expertise contributes to shaping the future of clinical research and advancing innovative treatments that improve patient lives worldwide.

Learn more about ICON and apply: ICON Careers