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Hiring Clinical Data Coordinator I & Clinical Trial Associate
ICON plc
Bangalore | Chennai | Trivandrum
Entry Level
Clinical Research
🏢 About ICON
ICON plc is a leading global Clinical Research Organization (CRO) supporting pharmaceutical and biotech companies in clinical trials, data management, and drug development.
📊 1. Clinical Data Coordinator I (CDC I)
- Domain: Clinical Data Management
- Develop eCRF & validation specs
- Perform data review & discrepancy management
- Raise & track queries
- Ensure ICH-GCP compliance
- Manage study documentation
📋 2. Clinical Trial Associate (CTA)
- Domain: Clinical Operations
- Assist in trial coordination
- Maintain TMF & regulatory documents
- Prepare ICF & CRF
- Track milestones & compliance
- Coordinate with teams
🎓 Eligibility
- B.Pharm / M.Pharm / BSc / MSc / Life Sciences
- Basic clinical research knowledge
- ICH-GCP understanding
- Good communication skills
💰 Salary (Estimated)
- CDC I: ₹3.5 – ₹6 LPA
- CTA: ₹3 – ₹5.5 LPA
📍 Job Locations
- Bangalore
- Chennai
- Trivandrum
- Hybrid flexibility
🎯 Why This Role is Important
- Entry into Clinical Research Industry
- Exposure to global trials
- Career path: CRA / CDM / PV
📚 Internal Resources (Must Read)
🎯 Interview Tips
- Revise ICH-GCP basics
- Understand clinical trial phases
- Prepare documentation questions
- Practice communication skills
📚 Practice:
📌 Note Before You Apply:
Read the job role carefully before applying. Choose CDC or CTA based on your interest.
Read the job role carefully before applying. Choose CDC or CTA based on your interest.
🚀 Job Application Links (ICON)
📌 Important Note Before You Apply:
Kindly read the full job description carefully for your selected role before applying. Ensure your profile, qualifications, and core competencies align with Clinical Data Management (CDM) data cleaning workflows, query management, clinical trial tracking, Trial Master File (TMF) maintenance, and ICH-GCP regulatory guidelines compliance standards before proceeding with your application on the ICON portal.
Kindly read the full job description carefully for your selected role before applying. Ensure your profile, qualifications, and core competencies align with Clinical Data Management (CDM) data cleaning workflows, query management, clinical trial tracking, Trial Master File (TMF) maintenance, and ICH-GCP regulatory guidelines compliance standards before proceeding with your application on the ICON portal.
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