Clinical Trial Assistant

ICON plc is a healthcare intelligence and clinical research organization seeking a Clinical Trial Administrator (Clinical Trial Assistant) to support clinical development activities. The role focuses on coordinating and administering clinical trials, maintaining documentation, and supporting study materials and reporting to help ensure smooth trial execution and compliance.

• 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 ensure 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 entitlements, health insurance options, retirement planning, Global 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, non-discriminatory workplace; reasonable accommodations available during the application process.