Clinical Trial Assistant

ICON plc is a global healthcare intelligence and clinical research organization focused on advancing clinical development. The Clinical Trial Administrator supports the coordination and administration of clinical trials, helping ensure compliant and smooth trial execution. This role contributes to organizing trial documentation, supporting study materials, and tracking trial progress.

• Assist in the coordination and administration of 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-related materials such as informed consent forms and case report forms.
• Collaborate with cross-functional teams to facilitate communication and support 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 Programme (LifeWorks), life assurance, and country-specific optional benefits (e.g., childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments).

• Inclusive workplace with equal opportunity and reasonable accommodations available.