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Hiring Clinical Trial Associate (CTA)
ICON plc
Bangalore
0–2 Years
Clinical Research
TMF & Documentation
Full-Time
🏢 About ICON plc
ICON plc is a leading global CRO supporting innovative drug development programs across multiple therapeutic areas. The organization partners with pharmaceutical, biotechnology, and medical device companies to deliver clinical development solutions worldwide.
📌 Job Overview
Position: Clinical Trial Associate (CTA)
Location: Bangalore, India
Experience: 0–2 Years
Qualification: Life Sciences / Pharmacy / Healthcare background
Industry: Clinical Research / CRO
🔬 Key Responsibilities
- Assist in coordination and administration of clinical trials
- Maintain Trial Master File (TMF) and essential documents
- Ensure compliance with ICH-GCP and regulatory requirements
- Support preparation of study documents (ICF, CRF, study files)
- Track trial milestones and performance metrics
- Coordinate with clinical operations & data management teams
- Support audit & inspection readiness documentation
🎓 Eligibility Criteria
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Nursing or related field
- Understanding of clinical trial processes & ICH-GCP
- Strong documentation & organizational skills
- Good communication & teamwork ability
- Internship experience in clinical research preferred
💰 Salary & Benefits
Estimated Salary: ₹3.8 – ₹6.5 LPA
- Health insurance & retirement benefits
- Annual leave & wellness support
- Global employee assistance program
- Life insurance & flexible benefits
⭐ Why Join ICON?
- Global CRO exposure
- Work on international clinical trials
- Strong career growth in clinical operations
- Supportive & inclusive work culture
📌 Note Before You Apply:
Read the responsibilities carefully. Understanding TMF management and clinical documentation improves your chances of selection.
Read the responsibilities carefully. Understanding TMF management and clinical documentation improves your chances of selection.
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