As a Clinical Trial Associate at ICON, you will support the design and analysis of clinical trials and interpretation of complex medical data to advance innovative treatments. You will coordinate and administer trials, ensure regulatory compliance, and maintain essential trial documentation. You will collaborate with cross‑functional teams to ensure smooth trial execution and contribute to tracking trial metrics and milestones. This role supports ICON’s mission to shape the future of clinical development by delivering high‑quality research with a focus on inclusion and well‑being.
Various annual leave entitlements
Health insurance offerings
Global Employee Assistance Programme LifeWorks
Life assurance
Flexible country‑specific optional benefits
Assist in coordination and administration of clinical trials with adherence to protocols and regulatory requirements
Maintain and organize study files,



essential documents, and regulatory submissions
Support preparation of study‑related materials (informed consent forms and case report forms)
Collaborate with cross‑functional teams to enable smooth trial execution
Contribute to tracking and reporting 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 attention to detail
Based in Rome and surroundings to reach client’s office

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📌 Clinical Trial Associate (Roma)
🏢 Altro
📍 Roma