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ICON Hiring Clinical Trial Associate (CTA)
Chennai
1–3 Years
Clinical Trials
CTA Role
🏢 About Company
ICON plc is a global clinical research organization (CRO) providing clinical development and commercialization services to pharmaceutical and biotechnology companies worldwide.
💼 Job Overview
- Role: Clinical Trial Associate (CTA)
- Location: Chennai (Office with Flex)
- Experience: 1–3 Years
- Job Type: Full-Time
- Industry: Clinical Research
📌 Key Responsibilities
- Support clinical trial coordination & documentation
- Maintain Trial Master File (TMF)
- Assist with ICF & CRF preparation
- Ensure compliance with ICH-GCP guidelines
- Track trial progress & milestones
- Collaborate with clinical teams
🎓 Eligibility
- Life Sciences / Pharmacy / Biotechnology degree
- 1–3 years clinical research experience
- Understanding of ICH-GCP
- Strong communication skills
💻 Required Skills
- Clinical trial documentation
- TMF management
- Regulatory compliance
- Attention to detail
- Team collaboration
💰 Salary & Benefits
- ₹3 – ₹6 LPA (Estimated)
- Health & life insurance
- Global work exposure
- Career growth in clinical research
🚀 Career Growth
- Clinical Research Associate (CRA)
- Clinical Operations Specialist
- Data Management Roles
- Regulatory Affairs
🎯 Interview Tips
- Revise ICH-GCP guidelines
- Understand TMF structure
- Know clinical trial phases
- Prepare scenario-based answers
- Be clear on CTA role responsibilities
📌 Note Before You Apply:
Kindly read the entire job description carefully before applying. Make sure your qualifications and experience align with the role requirements. Applying thoughtfully increases your chances of being shortlisted and creates a strong professional impression.
Kindly read the entire job description carefully before applying. Make sure your qualifications and experience align with the role requirements. Applying thoughtfully increases your chances of being shortlisted and creates a strong professional impression.
🚀 Job Application Link
📋 Study Coordination Checklist:
ICON's clinical operations team values precision in study tracking and administrative workflows. Before finalizing your form on their Workday system, verify that your resume clearly highlights your understanding of Trial Master File (eTMF) management, essential study document tracking, investigator site communication protocols, and global ICH-GCP frameworks.
ICON's clinical operations team values precision in study tracking and administrative workflows. Before finalizing your form on their Workday system, verify that your resume clearly highlights your understanding of Trial Master File (eTMF) management, essential study document tracking, investigator site communication protocols, and global ICH-GCP frameworks.
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