Clinical Trial Assistant

ICON plc is a global healthcare intelligence and clinical research organization seeking a Clinical Trial Administrator/Assistant to support the coordination and administration of clinical trials. The role focuses on maintaining trial documentation, supporting study materials, and enabling smooth trial execution in compliance with protocols and regulations.

• Assist in coordinating and administering clinical trials while ensuring compliance with study 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 smooth trial execution.
• Track and support reporting of clinical trial metrics and milestones.

• Bachelor's degree in a scientific or healthcare-related field.
• Prior experience 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 strong attention to detail.

• Benefits: competitive salary (amount not stated), annual leave entitlements, health insurance options, retirement planning offerings, Employee Assistance Programme (LifeWorks), life assurance, and optional benefits (may include childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments).

• Work environment: inclusive, non-discriminatory workplace; reasonable accommodations available.