Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Cdc Ii

Icon Plc
ICON PLC
5+ years
Not Disclosed
10 Jan. 22, 2026
Job Description
Job Type: Full Time Remote 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) – ICON India
Location: Chennai, India
Employment Type: Full-time
Work Mode: Office with Flex
Job ID: JR142313
Application Deadline: January 30, 2026


About ICON

ICON plc is a world-leading healthcare intelligence and clinical research organization, committed to innovation, quality, and inclusive collaboration. We provide advanced clinical research solutions globally, enabling the delivery of safe and effective therapies while fostering career growth for our employees.


Role Overview

ICON is seeking a Clinical Data Coordinator II (CDC II) to support clinical trial operations and data management. In this role, you will assist in managing study data, ensuring integrity, and supporting analysis and reporting activities. You will work closely with cross-functional teams, including clinical data scientists and project managers, contributing to the successful execution of clinical trials.


Key Responsibilities

  • Assist Data Management Study Leads in maintaining eCRFs, data validation specifications, and study-specific procedures.

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

  • Track and communicate study and task metrics to the project team and functional management.

  • Address data-related questions and recommend solutions.

  • Identify root causes of data issues and implement systematic resolutions.


Candidate Profile

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

  • 5+ years of experience in clinical data management within pharmaceutical or biotechnology environments.

  • Familiarity with clinical data management systems such as Medidata, Oracle RDC, or similar.

  • Strong attention to detail and ability to work effectively in a fast-paced, cross-functional environment.

  • Excellent communication and collaboration skills.

  • Knowledge of regulatory guidelines such as ICH-GCP is a plus.


Why Join ICON

  • Global Impact: Work on international clinical studies contributing to innovative therapies.

  • Career Development: Mentorship, tailored learning pathways, and opportunities for skill expansion.

  • Comprehensive Benefits: Health insurance, retirement planning, life assurance, flexible work options, and wellness initiatives.

  • Inclusive Culture: ICON fosters diversity, equity, and belonging, ensuring a supportive workplace environment.