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Clinical Trial Associate (CTA)
ICON plc
Chennai
Clinical Research
CTA Role
Clinical Operations
🏢 About ICON plc
ICON plc is a global healthcare intelligence and clinical research organization supporting pharmaceutical, biotechnology, and medical device companies in clinical development and drug safety. The company operates worldwide and plays a major role in advancing global clinical research.
📌 Job Overview
- Role: Clinical Trial Associate (CTA)
- Company: ICON plc
- Location: Chennai, India
- Employment Type: Full-time (Office with Flex)
- Department: Clinical Operations
- Job ID: JR141941
🔬 Key Responsibilities
- Assist in coordination and administration of clinical trials
- Maintain essential clinical trial documents and study files
- Support preparation of study documents such as ICFs and CRFs
- Ensure compliance with study protocols and GCP guidelines
- Track study timelines, milestones, and project activities
- Support regulatory submissions and documentation
- Coordinate communication across clinical study teams
🎓 Eligibility Criteria
- B.Pharm / M.Pharm / Pharm.D
- BSc / MSc Life Sciences
- Any Life Science or Health-related degree
- Understanding of clinical trial processes and GCP guidelines
- Strong organizational and communication skills
- Proficiency in MS Office (Excel required)
⭐ Benefits of Working at ICON
- Competitive salary and performance rewards
- Comprehensive health insurance benefits
- Retirement planning and financial support programs
- Employee Assistance Programme (TELUS Health)
- Flexible benefits including travel and wellness programs
- Inclusive and diverse global workplace
📌 Note Before You Apply:
Kindly read the entire job description carefully before applying. Understanding clinical trial documentation, GCP guidelines, and regulatory requirements will increase your chances of selection.
Kindly read the entire job description carefully before applying. Understanding clinical trial documentation, GCP guidelines, and regulatory requirements will increase your chances of selection.
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