ICON is hiring a Clinical Trial Associate for its clinical research team in Chennai, India. This full-time opportunity is suitable for candidates with a Bachelor’s degree in a scientific or healthcare-related field and an interest or experience in clinical research.
The ICON Clinical Trial Associate job involves supporting the coordination and administration of clinical trials, maintaining essential study documentation, assisting cross-functional teams, and helping ensure compliance with clinical trial protocols and regulatory requirements.
For candidates looking for Clinical Trial Associate jobs in Chennai, clinical research jobs in India, and ICON jobs for life science graduates, this role provides an opportunity to contribute to the development of innovative medicines and treatments.
Job Details
| Job Details | Information |
|---|---|
| Company | ICON |
| Job Role | Clinical Trial Associate |
| Job Location | Chennai, India |
| Work Type | Office With Flex |
| Employment Type | Full-time |
| Qualification | Bachelor’s Degree in Scientific or Healthcare-Related Field |
| Experience | Prior experience or strong interest in Clinical Research |
| Job ID | JR141941 |
| Posted On | September 9, 2026 |
| Estimated Salary | โน4.5โ8 LPA* |
About the Role
The Clinical Trial Associate at ICON will support the coordination and administration of clinical trials. The role focuses on maintaining clinical trial documentation, supporting study-related activities, coordinating with cross-functional teams, and tracking clinical trial metrics and milestones.
The successful candidate will work in a fast-paced clinical research environment and contribute to ensuring that clinical studies are conducted according to applicable protocols, regulations, and guidelines.
Key Responsibilities
As a Clinical Trial Associate, you will:
- Assist with the coordination and administration of clinical trials.
- Support compliance with study protocols and regulatory requirements.
- Maintain and organize clinical trial documentation and study files.
- Manage essential documents and regulatory submissions.
- Support the preparation of informed consent forms and case report forms.
- Coordinate with cross-functional teams to support smooth clinical trial execution.
- Assist in communication between relevant study stakeholders.
- Track and report clinical trial metrics and milestones.
- Support accurate documentation and efficient study administration.
Qualifications
Candidates applying for ICON Clinical Trial Associate jobs should have:
- Bachelor’s Degree in a scientific or healthcare-related field.
- Prior experience in clinical research or a strong interest in clinical research.
- Knowledge of clinical trial processes.
- Understanding of clinical research regulations and guidelines.
- Excellent organizational skills.
- Strong written and verbal communication skills.
- Ability to work collaboratively in a fast-paced environment.
- Strong attention to detail.
Eligible Degrees
B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Biotechnology, Life Sciences, Nursing, Medicine, or other Scientific and Healthcare-related degrees.
Key Skills for Clinical Trial Associates
Candidates may benefit from knowledge and skills in:
- Clinical Trial Coordination
- Clinical Trial Documentation
- Regulatory Compliance
- Clinical Research Processes
- Cross-functional Collaboration
- Case Report Forms (CRFs)
- Study File Management
- Communication and Organization
Benefits at ICON
ICON offers a comprehensive rewards and benefits package designed to support employee wellbeing and career development.
Benefits may include:
- Competitive base salary.
- Performance-related incentives.
- Health and wellbeing programs.
- Medical, dental, and vision coverage where applicable.
- Retirement and pension plans.
- Life assurance and disability coverage.
- Employee assistance programs.
- Wellbeing resources.
- Learning and development opportunities.
- Structured training and career development pathways.
How to Apply
