Clinical Trial Associate

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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