ICON Hiring Clinical Trial Associate (CTA) | B.Pharm, M.Pharm, Pharm.D & Life Sciences Graduates
ICON is hiring Clinical Trial Associates (CTA) for its Bangalore office. This opportunity is ideal for candidates from Pharmacy, Life Sciences, Biotechnology, Nursing, Healthcare, and Medical Sciences backgrounds who are looking to build careers in Clinical Research and Clinical Trial Management.
The role offers exposure to Clinical Operations, Trial Master File (TMF) Management, Regulatory Documentation, Study Start-up Activities, and Global Clinical Trial Execution within one of the world's leading CROs.
📋 Job Overview
| Particulars | Details |
|---|---|
| Position | Clinical Trial Associate (CTA) |
| Company | ICON |
| Location | Bangalore, Karnataka |
| Job Type | Full-Time |
| Work Model | Office With Flex |
| Experience | Freshers to Experienced |
| Industry | Clinical Research |
| Application Deadline | 02 June 2026 |
🏢 About ICON
ICON is a leading global healthcare intelligence and clinical research organization supporting pharmaceutical, biotechnology, and medical device companies worldwide. The company plays a key role in accelerating the development of innovative therapies and life-changing medicines.
📌 Key Responsibilities
- Assist in coordination and administration of clinical trials.
- Maintain and organize Trial Master Files (TMF).
- Support preparation of informed consent forms (ICFs) and CRFs.
- Ensure compliance with ICH-GCP guidelines and protocols.
- Support regulatory submissions and document management activities.
- Track study milestones and trial metrics.
- Collaborate with cross-functional teams.
- Support study start-up and ongoing trial activities.
🎓 Eligibility Criteria
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc (Life Sciences)
- M.Sc (Life Sciences)
- Biotechnology
- Nursing
- Healthcare
- Medical Sciences
- Related Scientific Disciplines
Experience:
- Freshers can apply.
- Prior Clinical Research experience preferred but not mandatory.
💡 Required Skills
- Clinical Trial Management
- Clinical Research Operations
- TMF Management
- Regulatory Documentation
- ICH-GCP Compliance
- Study Coordination
- CRF & ICF Documentation
- Project Coordination
- Microsoft Office
- Communication & Documentation Skills
🎁 Benefits Offered by ICON
- Competitive salary package.
- Performance-based incentives.
- Medical and health insurance.
- Life and disability coverage.
- Employee assistance programs.
- Learning and development opportunities.
- Structured career growth.
- Global clinical research exposure.
📄 Resume & Interview Preparation Tips
- Highlight Clinical Research, Documentation, TMF, and Study Coordination experience.
- Mention internships, projects, and research exposure.
- Add knowledge of ICH-GCP and Clinical Trial processes.
- Keep your resume ATS-friendly.
- Prepare for questions on Clinical Trials and Documentation.
📝 How to Apply
- Read the complete job description carefully.
- Prepare an updated ATS-friendly resume.
- Apply before the application deadline.
- Complete the 15-second countdown timer to unlock the application button.
🚀 Apply for ICON Clinical Trial Associate
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