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

📌 Clinical Trial Associate (Roma)
🏢 Altro
📍 Roma