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Cdc I / Cdc Ii

ICON
Freshers years
Not Disclosed
Bangalore, Trivandrum, India
10 May 20, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Overview

Job Title: CDC I / CDC II (Clinical Data Coordinator)
Company: ICON plc
Job Requisition ID: JR137696
Locations:

  • Bangalore

  • Thiruvananthapuram

Work Mode: Office With Flex
Employment Type: Full-time
Posted: 9 days ago


About the Company

ICON plc is a global clinical research and healthcare intelligence organization focused on advancing clinical development and innovative healthcare solutions.

The company promotes:

  • Innovation and excellence

  • Inclusive workplace culture

  • Employee well-being and professional growth


Role Summary

The CDC I / CDC II role involves supporting clinical data management activities for clinical trials. The Clinical Data Coordinator will assist in reviewing and validating clinical data, managing study documentation, and collaborating with cross-functional teams to ensure data quality and study timelines are maintained.


Key Responsibilities

1. Clinical Data Management Support

  • Assist Data Management Study Leads in:

    • eCRF development

    • Data Validation Specifications

    • Study-specific procedures

2. Data Review & Validation

  • Review:

    • Clinical trial data

    • Third-party data

  • Ensure data accuracy based on edit specifications and review plans

3. Query Management

  • Generate and send clear, concise, and accurate queries to investigational sites

  • Support issue resolution and data clarification processes

4. Cross-Functional Communication

  • Collaborate with:

    • Clinical Data Scientists

    • Functional management teams

    • Project stakeholders

5. Study Documentation & Timelines

  • Support filing and archiving of study documents

  • Ensure project activities are completed within timelines

  • Assist with study coordination activities as required


Required Qualifications

Educational Qualification

Bachelor’s degree in:

  • Life Sciences

  • Healthcare

  • Related fields

Technical Knowledge

  • Basic understanding of Clinical Data Management in:

    • Pharmaceutical industry

    • Biotechnology industry

Software Knowledge

Familiarity with:

  • Medidata

  • Oracle RDC

  • Similar clinical data management systems

Skills Required

  • Strong attention to detail

  • Ability to work in fast-paced environments

  • Excellent communication skills

  • Team collaboration abilities

Preferred Knowledge

  • Understanding of:

    • ICH-GCP guidelines

    • Regulatory standards


Benefits Offered

Health & Wellness

  • Health insurance options for employees and families

  • Global Employee Assistance Programme (TELUS Health)

  • Life assurance coverage

Work-Life Balance

  • Annual leave entitlements

  • Flexible work environment

Financial & Lifestyle Benefits

  • Retirement planning support

  • Childcare vouchers

  • Discounted gym memberships

  • Subsidized travel passes

  • Health assessments

  • Country-specific optional benefits


Work Culture & Inclusion

ICON plc is committed to:

  • Diversity and inclusion

  • Equal employment opportunities

  • Accessible workplace practices

  • Harassment-free work culture

Reasonable accommodations are available for candidates with medical conditions or disabilities during the application process.