Clinical Trial Associate

ICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Clinical Trial Associate to join its diverse team. The role supports the coordination, documentation, and operational execution of clinical trials to help advance innovative treatments and therapies.

• Assist in the coordination and administration of clinical trials, ensuring 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 optional country-specific benefits (e.g., childcare vouchers, bike schemes, discounted gym memberships, subsidized travel passes, health assessments).

• Inclusive, equal-opportunity workplace with accommodations available for candidates with disabilities.