ICON plc Hiring Clinical Data Coordinator I (CDC I) – Hybrid Clinical Data Management Job Opportunity in India 2026

Are you looking to start or advance your career in Clinical Data Management (CDM)? Here’s an exciting opportunity with ICON plc, one of the world’s leading Clinical Research Organizations (CROs). The company is currently hiring for the position of Clinical Data Coordinator I (CDC I) across multiple locations in India.

This role offers an excellent opportunity for Life Sciences, Pharmacy, Biotechnology, and Healthcare graduates who are interested in clinical research, data management, and global healthcare projects.

About ICON plc

ICON plc is a globally recognized healthcare intelligence and clinical research organization that supports pharmaceutical, biotechnology, and medical device companies in bringing innovative therapies to patients worldwide.

With operations spanning several countries, ICON focuses on delivering high-quality clinical development solutions while maintaining its core values:

Integrity
Collaboration
Inclusion
Agility

Working at ICON provides professionals with exposure to international clinical trials, advanced technologies, and global healthcare standards.

Job Summary

Details	Information
Company Name	ICON plc
Position	Clinical Data Coordinator I (CDC I)
Job ID	JR153061
Employment Type	Full-Time
Work Mode	Office With Flex (Hybrid)
Industry	Clinical Research / CRO
Experience	Freshers & Experienced
Location	Bangalore, Chennai, Trivandrum

Work Locations

Selected candidates may be based at any of the following ICON offices:

Bangalore, Karnataka
Chennai, Tamil Nadu
Trivandrum, Kerala

The hybrid work model allows employees to enjoy flexibility while maintaining collaboration with project teams.

Key Responsibilities

As a Clinical Data Coordinator I, you will support clinical trial data management activities and ensure the accuracy and quality of study data.

Study Setup Activities

Assist in creating Electronic Case Report Forms (eCRFs)
Support development of Data Validation Specifications (DVS)
Contribute to Study Specific Procedures (SSPs)

Clinical Data Review

Review patient and third-party clinical data
Verify data consistency and quality
Identify discrepancies and data issues
Generate and track data queries

Documentation & Compliance

Maintain study-related records and documentation
Support filing and archiving activities
Ensure adherence to regulatory and project requirements

Cross-Functional Collaboration

Work closely with Clinical Data Scientists
Coordinate with project teams and stakeholders
Participate in study-related discussions and meetings

Educational Qualification

Candidates should possess:

Bachelor’s Degree in Life Sciences
B.Pharm
Biotechnology
Healthcare-related disciplines
Other relevant scientific fields

Skills Required

Ideal candidates should have:

Basic understanding of Clinical Data Management
Knowledge of Electronic Data Capture (EDC) systems
Familiarity with Medidata Rave, Oracle RDC, or similar tools
Strong communication skills
Attention to detail
Problem-solving ability
Time management skills

Preferred Knowledge

Candidates with exposure to the following areas will have an added advantage:

ICH-GCP Guidelines
Clinical Research Processes
Regulatory Compliance
Clinical Trial Documentation

Why Consider a Career in Clinical Data Management?

Clinical Data Management is one of the fastest-growing sectors in the pharmaceutical and biotechnology industries.

Benefits include:

Strong career growth opportunities
Global work exposure
High demand across CROs and pharmaceutical companies
Opportunities to work on international clinical trials
Attractive salary progression

Potential career paths include:

Clinical Data Coordinator
Clinical Data Associate
Clinical Data Scientist
Clinical Data Lead
Data Management Project Manager

How to Apply

Interested candidates can apply through the official ICON careers portal using the link below:

Apply Here:
https://icon.wd3.myworkdayjobs.com/broadbean_external/job/India-Bangalore/CDC-I_JR153061-1

Tips to Increase Your Selection Chances

Before applying:

Update your resume with relevant skills and certifications.
Highlight any Clinical Research or CDM training.
Mention knowledge of ICH-GCP guidelines.
Include internships, projects, or certifications related to clinical research.
Proofread your resume carefully before submission.

Frequently Asked Questions (FAQs)

Is this position open for freshers?

Yes. Candidates with relevant educational backgrounds and foundational knowledge of clinical research and data management can apply.

Is the job remote?

The role follows ICON’s Office With Flex model, which combines office work with flexible working arrangements.

Which degree holders can apply?

Life Sciences, Pharmacy, Biotechnology, Healthcare, and related graduates are eligible.

What software knowledge is preferred?

Knowledge of Medidata Rave, Oracle RDC, and other Electronic Data Capture (EDC) systems is beneficial.

What is the career scope after joining as CDC I?

Professionals can progress toward Clinical Data Scientist, Data Management Lead, Clinical Trial Lead, and Project Management positions.

Disclaimer

The recruitment information provided in this article is based on the official job posting available at the time of publishing. Candidates are advised to verify all details through the official company career page before applying.