Clinical Trial Administrator

Role & Responsibilities
• Assist in the coordination and administration of clinical trials
• Ensure compliance with study protocols and regulatory requirements
• Maintain and organize clinical trial documentation and regulatory submissions
• Support preparation of study-related materials such as informed consent forms and case report forms
• Collaborate with cross-functional teams for smooth trial execution
• Track and report clinical trial metrics and milestones to management

Qualification
• Bachelor’s degree in Life Sciences, Pharmacy, or healthcare-related field

Experience
• Freshers or candidates with prior experience in clinical trials

Skills
• Strong understanding of GCP guidelines and clinical trial processes
• Excellent organizational, communication, and multitasking skills
• Ability to work in a fast-paced, collaborative environment

Perks & Benefits
• Comprehensive health insurance plans for employees and families
• Competitive retirement and savings plans
• Generous annual leave and flexible working options
• Global Employee Assistance Program (TELUS Health)
• Country-specific benefits (gym memberships, travel passes, childcare vouchers)
• Inclusive workplace fostering diversity, equity, and belonging

About the Company
• ICON plc, a global leader in healthcare intelligence and clinical research
• Provides cutting-edge solutions in clinical development
• Offers a supportive and inclusive workplace focused on career growth