Clinical Trial Assistant

ICON plc is a healthcare intelligence and clinical research organization seeking a Clinical Trial Administrator/Assistant to support clinical trial operations. The role focuses on coordinating trial activities, maintaining documentation, and supporting study materials to enable compliant and 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 a 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 entitlements, health insurance options, retirement planning, employee assistance program (LifeWorks), and life assurance.

• Optional country-specific benefits may include childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, and health assessments.