Overview
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.
Retribuzione / Benefits
Competitive base salary
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways
Responsabilità
Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
Ensure protocol compliance, data integrity, and patient safety throughout the trial process




Collaborate with investigators and site staff to facilitate smooth study conduct
Perform data review and resolution of queries to maintain high-quality clinical data
Contribute to the preparation and review of study documentation, including protocols and clinical study reports
Requisiti fondamentali
Bachelor's degree in a scientific or healthcare-related field
Minimum of 2 years of experience as a Clinical Research Associate after being certified as per Italian Decree
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Strong organizational and communication skills, with attention to detail
Ability to work independently and collaboratively in a fast-paced environment
Employment eligibility to work in the role's country
strong communication
attention to detail
team collaboration
clinical trial monitoring
data review and query resolution
ICH-GCP knowledge

📌 Clinical Research Associate (Milano)
🏢 Icon Clinical
📍 Milano