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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.
