ICON plc, a global leader in clinical research and healthcare intelligence, is hiring for the position of Clinical Site Associate across India locations including Chennai, Bengaluru, and Trivandrum. This is an excellent opportunity for candidates looking to build a career in clinical research, clinical trial site management, and life sciences operations.
The Clinical Site Associate job at ICON plc India focuses on supporting clinical trial site management activities, ensuring compliance, documentation accuracy, and smooth coordination between clinical research associates (CRAs), investigators, and internal teams.
This role is highly suitable for freshers or early professionals aiming to enter the clinical research industry in India.
Key Responsibilities โ Clinical Site Associate ICON
As a Clinical Site Associate in clinical research, your core responsibilities include:
- Supporting site activation and start-up activities in clinical trials
- Managing and tracking essential regulatory and study documents
- Maintaining accurate updates in clinical trial management systems (CTMS)
- Coordinating with CRAs and site staff for query resolution
- Scheduling and organizing site visits, meetings, and follow-ups
- Assisting in clinical trial documentation and audit readiness
- Supporting site payment tracking and administrative coordination
- Ensuring compliance with Good Clinical Practice (GCP) standards
- Contributing to process improvement in site management workflows
Required Qualifications
To apply for the ICON Clinical Site Associate job in India, candidates should meet the following requirements:
- Bachelorโs degree in Life Sciences, Pharmacy, Healthcare, Biotechnology, or Business Administration
- Basic understanding of clinical research processes (preferred but not mandatory)
- Strong attention to detail and documentation accuracy
- Good communication skills (written and verbal)
- Proficiency in MS Office (Excel, Word, Outlook)
- Ability to manage multiple tasks in a regulated environment
- Team-oriented mindset with strong organizational skills
Preferred Skills
- Exposure to clinical trials or healthcare administration
- Knowledge of GCP guidelines and clinical trial documentation
- Experience with CTMS or eTMF systems (added advantage)
- Problem-solving and coordination abilities
Benefits of Working at ICON plc
ICON offers a globally competitive work environment with strong employee support systems:
- Competitive salary package in the clinical research domain
- Health insurance coverage for employees and families
- Paid annual leave and flexible benefits
- Global Employee Assistance Programme (24/7 support)
- Retirement and savings planning options
- Hybrid/office-based flexible working model
- Learning and career development opportunities in clinical trials
- Inclusive and diversity-driven workplace culture
Salary Details
- Expected Salary Range: โน4 LPA โ โน7 LPA (Approx.)
- Based on experience, skills, and location (Chennai / Bengaluru / Trivandrum)
How to Apply
