In this role, you contribute to the design and analysis of clinical trials within ICON's sponsor-dedicated model.
You will monitor sites, ensure protocol adherence, data integrity, and patient safety, and collaborate with investigators to ensure smooth study conduct.
You'll review data, resolve queries, and help prepare study documents to support trial quality.
This is a role that combines hands-on monitoring with cross-functional teamwork to advance treatments for patients globally.Health and wellbeing programmes including medical, dental, and vision coverage where applicableRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysConduct site qualification, initiation, monitoring, and close-out visits for clinical trialsEnsure protocol compliance, data integrity,



and patient safety throughout the trial processCollaborate with investigators and site staff to facilitate smooth study conductPerform data review and resolution of queries to maintain high-quality clinical dataContribute to the preparation and review of study documentation, including protocols and clinical study reportsBachelor's degree in a scientific or healthcare-related field xysqume Minimum of 2 years of experience as a Clinical Research Associate after being certified as per Italian DecreeIn-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelinesStrong organizational and communication skills, with attention to detailAbility to work independently and collaboratively in a fast-paced environmentEmployment eligibility to work in the role's country#J-*****-Ljbffr

📌 Clinical Research Associate (Bardi)
🏢 Experteer Italy
📍 Bardi