ICON plc, a global leader in clinical research and healthcare intelligence, is hiring a Site Specialist II in Chennai or Bangalore. This is your opportunity to contribute to groundbreaking clinical trials that improve global healthcare outcomes.
If you’re passionate about clinical operations, site activation, and trial documentation, this role offers the perfect environment to enhance your expertise within a world-class research organization.
Key Responsibilities
As a Site Specialist II, you will:
- Support site activation activities and vendor coordination (eCRF, IVRS).
- Manage CDP and submission documentation, ensuring accuracy and compliance.
- Maintain study trackers to monitor milestones and deliverables.
- Collaborate with CRAs, CTAs, and Site Partners to enhance trial efficiency.
- Participate in study review meetings for risk mitigation and planning.
- Ensure Trial Master File (TMF) quality and completeness.
- Adhere to ICH-GCP guidelines, ICON SOPs/WPs, and local regulations.
- Perform additional tasks to support project and departmental goals.
Required Qualifications
- Education: Bachelor’s degree in Life Sciences or a related field.
- Experience: Minimum 3 years in clinical research, site operations, or documentation management.
- Knowledge: Understanding of clinical trial processes, vendor systems (eCRF, IVRS), and documentation workflows.
- Skills: Strong organizational, documentation, and communication skills.
- Compliance: Familiarity with ICH-GCP and regulatory requirements.
Why Join ICON plc?
ICON plc is committed to fostering an inclusive and high-performing culture. The company values professional growth, employee well-being, and work-life balance.
Employee Benefits Include:
- Competitive annual leave and health insurance packages.
- Retirement planning and financial wellness programs.
- Access to TELUS Health – Global Employee Assistance Programme.
- Life assurance and flexible country-specific perks (e.g., childcare vouchers, gym memberships, travel subsidies).
How to Apply
