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ICON
5 years
preferred by company
10 Jan. 23, 2026
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 II (CDC II) – Clinical Data Management

Job Requisition ID: JR142313
Employment Type: Full Time
Work Mode: Office-Based with Flexible Work Options
Location: Chennai, India
Experience Required: Minimum 5 Years
Application Deadline: January 30, 2026

Job Overview

ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a skilled Clinical Data Coordinator II (CDC II) to support global clinical trials through high-quality clinical data management activities. This role is critical to ensuring data accuracy, integrity, and regulatory compliance across the clinical development lifecycle.

The Clinical Data Coordinator II will work closely with study leads and cross-functional teams to manage clinical and third-party data, resolve data issues, and support efficient study execution.

Key Responsibilities

Clinical Data Management Support

  • Assist the Data Management Study Lead in maintaining electronic case report forms (eCRFs), data validation specifications, and study-specific procedures.

  • Manage reconciliation of clinical and third-party data in accordance with edit specifications and data review plans.

Data Review & Issue Resolution

  • Identify, analyze, and resolve data discrepancies by determining root causes and implementing systematic solutions.

  • Address data-related queries from study teams and recommend effective corrective actions.

Study Tracking & Reporting

  • Track study-level and task-level metrics and communicate status updates to clinical data scientists, project teams, and functional management.

  • Support data review activities to ensure timely and accurate study deliverables.

Cross-Functional Collaboration

  • Collaborate with clinical operations, biostatistics, and data management teams to ensure data quality and alignment with study requirements.

Required Qualifications & Experience

  • Bachelor’s degree in Life Sciences, Healthcare, Clinical Research, or a related discipline.

  • Minimum 5 years of relevant experience in clinical data management within a pharmaceutical, biotechnology, or CRO environment.

  • Intermediate-level expertise in clinical data management processes and workflows.

Technical Skills & Knowledge

  • Hands-on experience with clinical data management systems such as Medidata Rave, Oracle RDC, or similar EDC platforms.

  • Strong understanding of clinical trial data standards and lifecycle.

  • Knowledge of global regulatory guidelines, including ICH-GCP, is highly desirable.

Skills & Competencies

  • Strong attention to detail with excellent analytical and problem-solving skills.

  • Ability to work effectively in a fast-paced, regulated clinical research environment.

  • Clear and effective communication skills with the ability to collaborate across cross-functional teams.

  • Proven capability to manage multiple data-related activities while meeting project timelines.

Why Join ICON

ICON offers a collaborative, inclusive, and performance-driven work environment that supports professional development and long-term career growth. Employees benefit from competitive compensation, flexible work arrangements, and comprehensive benefits designed to promote well-being and work-life balance.

ICON is an equal opportunity employer committed to diversity, equity, and inclusion across its global workforce.