Clinical Trial Assistant

ICON plc is a global healthcare intelligence and clinical research organization seeking a Clinical Trial Administrator/Assistant to support the coordination and administration of clinical trials. The role focuses on maintaining trial documentation, supporting study materials, and helping teams execute trials in compliance with protocols and regulations.

• Assist in the coordination and administration of clinical trials to ensure 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.
• Work 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 collaborate 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 flexible optional benefits (e.g., childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments) depending on country.

• Inclusive workplace and reasonable accommodation available during application process.