Global clinical research organization ICON is inviting applications for the position of Clinical Trial Associate (CTA) in Bangalore, India. This opportunity is ideal for candidates with a background in Life Sciences, Pharmacy, Healthcare, Nursing, Biotechnology, or other scientific disciplines who are interested in building a career in clinical research and clinical trial management.
The Clinical Trial Associate role offers exposure to clinical trial operations, regulatory compliance, study documentation, and cross-functional collaboration within one of the world’s leading Contract Research Organizations (CROs). Candidates with prior clinical research experience or a strong interest in clinical trials are encouraged to apply.
About ICON
ICON is a leading global healthcare intelligence and clinical research organization dedicated to helping pharmaceutical, biotechnology, and medical device companies accelerate the development of innovative medicines and treatments. With operations across multiple countries, ICON supports clinical trials that bring life-changing therapies to patients worldwide.
Job Details
| Particulars | Details |
|---|---|
| Position | Clinical Trial Associate (CTA) |
| Company | ICON |
| Job Location | Bangalore, Karnataka, India |
| Job Type | Full-Time |
| Work Model | Office With Flex |
| Experience | Freshers to Experienced |
| Industry | Clinical Research |
| Application Deadline | 02 June 2026 |
Key Responsibilities of Clinical Trial Associate
As a Clinical Trial Associate at ICON, you will support clinical trial operations and ensure studies are conducted according to regulatory and protocol requirements.
Responsibilities include:
- Assisting in the coordination and administration of clinical trials.
- Maintaining and organizing Trial Master Files (TMF) and essential study documents.
- Supporting preparation of informed consent forms (ICFs), case report forms (CRFs), and study-related documentation.
- Ensuring compliance with clinical trial protocols, ICH-GCP guidelines, and regulatory requirements.
- Collaborating with cross-functional teams for smooth clinical trial execution.
- Tracking study milestones, deliverables, and clinical trial metrics.
- Supporting regulatory submissions and document management activities.
- Participating in study start-up and ongoing trial support activities.
Required Qualifications
Candidates applying for this Clinical Trial Associate job should possess:
- Bachelor’s degree in Pharmacy, Life Sciences, Biotechnology, Nursing, Healthcare, Medical Sciences, or related scientific discipline.
- Prior clinical research experience is preferred but not mandatory.
- Strong interest in clinical trial operations and clinical development.
- Understanding of clinical trial processes and regulations.
- Familiarity with ICH-GCP guidelines is advantageous.
- Excellent organizational and documentation skills.
- Strong verbal and written communication abilities.
- Ability to work in a fast-paced collaborative environment.
- Attention to detail and quality-focused mindset.
- Willingness to travel approximately 10% if required.
Skills Required
Clinical trial management, Clinical research operations, Trial Master File (TMF) management, Regulatory documentation, ICH-GCP compliance, Clinical study coordination, Study start-up activities, Case report forms (CRF), Informed consent process, Regulatory submissions, Microsoft Office, Communication skills, Documentation management, Project coordination, Cross-functional collaboration, Data tracking and reporting.
Salary and Benefits
The expected salary for a Clinical Trial Associate in Bangalore typically ranges between ₹4.5 LPA and ₹8.5 LPA, depending on qualifications, experience, and interview performance.
ICON offers:
- Competitive salary package
- Performance-based incentives
- Medical and health insurance benefits
- Life and disability coverage
- Employee assistance programs
- Retirement and pension benefits
- Learning and development programs
- Structured career growth opportunities
- Global clinical research exposure
- Inclusive and collaborative work culture
Why Join ICON?
ICON is recognized globally for delivering high-quality clinical research services and supporting innovative drug development programs. Joining ICON provides professionals with valuable experience in clinical trial management, regulatory compliance, clinical operations, and global study execution.
For candidates aspiring to build a long-term career in Clinical Research, Clinical Operations, Clinical Trial Management, CRA, CTA, TMF Management, Regulatory Affairs, or Clinical Data Management, this opportunity offers an excellent foundation.
How to Apply
