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Cdc I / Cdc Ii

ICON
0-2 years
Not Disclosed
Bangalore, Trivandrum, India
10 May 13, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Clinical Monitoring, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems, Clinical Trials, Collaboration, Data Integrity, Decision Making Skills, Lifesciences, 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

Company Overview

ICON plc is a world-leading healthcare intelligence and clinical research organization supporting pharmaceutical, biotechnology, medical device, and public health organizations in advancing clinical development and improving patient outcomes.


Job Details

Category

Details

Job Title

Clinical Data Coordinator (CDC I / CDC II)

Company

ICON plc

Department

Clinical Data Management

Industry

Clinical Research / Pharmaceutical / Biotechnology

Employment Type

Full-Time

Experience Level

Entry-Level / Early Career

Education Required

Bachelor’s Degree

Preferred Field

Life Sciences / Healthcare / Related Discipline


Role Summary

The Clinical Data Coordinator (CDC I / CDC II) supports clinical data management activities within clinical trials. The role involves reviewing clinical and third-party data, assisting in electronic Case Report Form (eCRF) development, issuing data queries, supporting study documentation, and ensuring data quality and regulatory compliance.

The position requires strong attention to detail, familiarity with clinical data systems, and collaboration with cross-functional clinical research teams.


Key Responsibilities

1. Clinical Data Management Support

  • Assist the Data Management Study Lead in:

    • eCRF development

    • Data Validation Specifications

    • Study-Specific Procedures

  • Support clinical trial data management activities.


2. Data Review & Validation

  • Review:

    • Clinical trial data

    • Third-party/vendor data

  • Validate data according to:

    • Edit specifications

    • Data review plans

  • Ensure data accuracy, consistency, and completeness.


3. Query Management

  • Generate and issue:

    • Clear

    • Accurate

    • Concise queries

  • Communicate data discrepancies to investigational sites for resolution.

  • Track and support timely query closure.


4. Documentation & Study Support

  • Support project timelines through:

    • Filing study documentation

    • Archiving records

    • Query dispatch activities

  • Maintain organized and audit-ready documentation.


5. Cross-Functional Collaboration

  • Communicate effectively with:

    • Clinical Data Scientists

    • Data Management teams

    • Functional management

    • Cross-functional study teams

  • Contribute to efficient project execution.


Required Qualifications

Educational Requirements

  • Bachelor’s Degree in:

    • Life Sciences

    • Healthcare

    • Related scientific discipline


Experience & Knowledge

  • Basic understanding of:

    • Clinical Data Management

    • Clinical trial processes

    • Pharmaceutical or biotechnology industry operations

  • Knowledge of:

    • eCRF processes

    • Clinical data review workflows


Technical Skills

  • Familiarity with clinical data management systems such as:

    • Medidata

    • Oracle RDC

    • Similar CDMS platforms

  • Basic understanding of:

    • Data validation

    • Query management

    • Clinical databases


Regulatory Knowledge

  • Familiarity with:

    • ICH-GCP guidelines

    • Clinical research standards

  • Regulatory knowledge is considered an advantage.


Soft Skills

  • Strong attention to detail

  • Organizational skills

  • Ability to work in fast-paced environments

  • Good communication skills

  • Team collaboration abilities

  • Time management and multitasking capability


Preferred Candidate Profile

Ideal candidates may have interest or experience in:

  • Clinical Data Management

  • Clinical Research

  • Electronic Data Capture (EDC)

  • eCRF Development

  • Clinical Trial Operations

  • Data Validation

  • Query Management

  • CRO environments

  • Pharmaceutical or Biotechnology companies


Benefits Offered

Compensation & Rewards

  • Competitive salary package

  • Performance recognition programs


Health & Wellbeing

  • Comprehensive health insurance options

  • Employee Assistance Programme (TELUS Health)

  • Life assurance coverage

  • Wellness initiatives


Work-Life Balance

  • Annual leave entitlements

  • Flexible employee benefits

  • Family-focused support policies


Financial & Lifestyle Benefits

  • Retirement planning programs

  • Childcare vouchers

  • Bike purchase schemes

  • Discounted gym memberships

  • Subsidized travel passes

  • Health assessments


Diversity & Inclusion

ICON plc is committed to fostering an inclusive and accessible work environment and provides equal employment opportunities regardless of:

  • Race

  • Religion

  • Gender

  • Sexual orientation

  • Gender identity

  • National origin

  • Disability

  • Veteran status