Clinical Trial Assistant

ICON plc is a global healthcare intelligence and clinical research organization supporting the development of new treatments and therapies. The Clinical Trial Administrator/Assistant role supports the coordination and administration of clinical trials, ensuring documentation quality and regulatory compliance to enable smooth trial execution.

• 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 smooth trial execution.
• Track and report 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.

• Competitive salary (amount not specified).

• Benefits may include annual leave, health insurance options, retirement planning, Employee Assistance Program (LifeWorks), life assurance, and optional country-specific benefits (e.g., childcare vouchers, bike schemes, gym discounts, subsidized travel passes, health assessments).

• Inclusive, non-discriminatory workplace with reasonable accommodations available during application and employment.