Global clinical research leader ICON plc is hiring for the position of Clinical Trial Associate (Clinical Trial Administrator) in Chennai, India. This opportunity is ideal for Life Sciences, Pharmacy, Biotechnology, Nursing, and Healthcare graduates looking to build a career in clinical research and clinical trial management.
Candidates with a strong interest in clinical trials, regulatory documentation, and study coordination can apply for this exciting role at one of the world’s leading Contract Research Organizations (CROs).
About ICON
ICON is a global healthcare intelligence and clinical research organization dedicated to accelerating the development of innovative medicines and therapies. The company partners with pharmaceutical, biotechnology, and medical device organizations worldwide to improve patient outcomes through advanced clinical research solutions.
The organization is known for its culture of integrity, collaboration, agility, and inclusion, providing employees with excellent career growth opportunities in the clinical research industry.
Job Details
| Particulars | Details |
|---|---|
| Position | Clinical Trial Associate |
| Department | Clinical Operations |
| Company | ICON plc |
| Location | Chennai, Tamil Nadu, India |
| Employment Type | Full-Time |
| Work Mode | Office with Flex |
| Industry | Clinical Research / CRO |
| Experience | Freshers & Experienced Candidates May Apply |
Key Responsibilities
As a Clinical Trial Associate at ICON, you will:
- Assist in the coordination and administration of clinical trials.
- Ensure compliance with study protocols and regulatory requirements.
- Maintain and organize Trial Master Files (TMF) and essential study documentation.
- Support preparation of informed consent forms, study materials, and case report forms.
- Coordinate with cross-functional clinical research teams.
- Track study milestones and clinical trial metrics.
- Support regulatory submission activities and document management.
- Facilitate communication between study teams and stakeholders.
- Ensure accurate documentation throughout the clinical trial lifecycle.
Required Qualifications
Candidates should possess:
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Nursing, Healthcare, or a related scientific field.
- Prior experience in clinical research is preferred but not mandatory.
- Strong interest in clinical trial operations and clinical development.
- Understanding of GCP (Good Clinical Practice) guidelines.
- Knowledge of clinical trial processes and regulatory requirements.
- Excellent organizational and communication skills.
- Strong attention to detail and documentation accuracy.
- Ability to work collaboratively in a fast-paced environment.
Preferred Skills
- Clinical trial documentation management
- Regulatory compliance knowledge
- Clinical research coordination
- Data tracking and reporting
- Team collaboration
- Microsoft Office proficiency
- Problem-solving abilities
Salary and Benefits
Based on current market standards for Clinical Trial Associate roles in India, the expected salary range is:
₹4.5 LPA – ₹7.5 LPA
Additional benefits may include:
- Competitive compensation package
- Performance-based incentives
- Medical and health insurance coverage
- Dental and vision benefits (where applicable)
- Retirement and pension plans
- Life insurance coverage
- Employee assistance programs
- Learning and development opportunities
- Structured career progression pathways
- Flexible work arrangements
Why Join ICON?
Working at ICON provides exposure to global clinical trials, international regulatory standards, and innovative drug development programs. Employees gain valuable experience in:
- Clinical trial management
- Regulatory compliance
- Study documentation
- Global healthcare research
- Cross-functional project collaboration
This role serves as an excellent entry point for candidates aspiring to become Clinical Research Associates (CRAs), Clinical Trial Managers, or Clinical Project Managers.
How to Apply
