ppAs 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. /pulliVarious annual leave entitlements /liliHealth insurance offerings /liliGlobal Employee Assistance Programme LifeWorks /liliLife assurance /liliFlexible country‑specific optional benefits /liliAssist in coordination and administration of clinical trials with adherence to protocols and regulatory requirements /liliMaintain and organize study files,



essential documents, and regulatory submissions /liliSupport preparation of study‑related materials (informed consent forms and case report forms) /liliCollaborate with cross‑functional teams to enable smooth trial execution /liliContribute to tracking and reporting clinical trial metrics and milestones /liliBachelor's degree in a scientific or healthcare‑related field /liliPrior experience or strong interest in clinical research /liliKnowledge of clinical trial processes, regulations, and guidelines /liliExcellent organizational and communication skills /liliAbility to work collaboratively in a fast‑paced environment with attention to detail /liliBased in Rome and surroundings to reach client’s office /li /ul /p #J-18808-Ljbffr

📌 Clinical Trial Associate (Roma)
🏢 Experteer Italy
📍 Roma