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 role supports the coordination and administration of clinical trials, ensuring documentation quality and regulatory compliance. This position works with cross-functional teams to help trials run smoothly and to track trial progress and metrics.

• 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 help report clinical trial metrics and milestones.

• Bachelor's degree in a scientific or healthcare-related field.

• Prior experience in clinical research 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 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 employment and accommodations available for disabilities/medical conditions during the application process.