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 entitlementsHealth insurance offeringsGlobal Employee Assistance Programme LifeWorksLife assuranceFlexible country‑specific optional benefitsAssist in coordination and administration of clinical trials with adherence to protocols and regulatory requirementsMaintain and organize study files,



essential documents, and regulatory submissionsSupport preparation of study‑related materials (informed consent forms and case report forms)Collaborate with cross‑functional teams to enable smooth trial executionContribute to tracking and reporting clinical trial metrics and milestonesBachelor's degree in a scientific or healthcare‑related fieldPrior experience or strong interest in clinical researchKnowledge of clinical trial processes, regulations, and guidelinesExcellent organizational and communication skillsAbility to work collaboratively in a fast‑paced environment with attention to detailBased in Rome and surroundings to reach client’s office#J-18808-Ljbffr

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