Clinical Trial Assistant

ICON plc is a healthcare intelligence and clinical research organization seeking a Clinical Trial Administrator to join its diverse team. The role supports the coordination and administration of clinical trials to ensure compliant, smooth execution and contribute to advancing new treatments.

• Assist in coordinating and administering clinical trials in compliance with protocols and regulatory requirements
• Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions
• Support preparation of study materials such as informed consent forms and case report forms
• Collaborate with cross-functional teams to facilitate communication and ensure smooth trial execution
• Track and report clinical trial metrics and milestones

• Bachelor’s degree in a scientific or healthcare-related field

• Prior experience in, or strong interest in, clinical research

• Knowledge of clinical trial processes, regulations, and guidelines

• Excellent organizational and communication skills

• Ability to work collaboratively in a fast-paced environment with attention to detail

• Competitive salary (amount not specified)

• Benefits may include annual leave entitlements, health insurance offerings, retirement planning, Employee Assistance Programme (LifeWorks), life assurance, and flexible optional benefits (e.g., childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments)

• Inclusive, equal-opportunity workplace with reasonable accommodations available