Overview
As a CRA II at ICON, you contribute to designing and analyzing clinical trials, ensuring data quality and patient safety while supporting investigators and site staff.
You'll work cross-functionally to monitor trials, resolve data queries, and prepare key study documents.
This role sits at the heart of advancing new medicines, offering opportunities to impact trial conduct and regulatory compliance.
You will travel ~60% to sites and collaborate in a fast-paced, mission-driven environment.
Retribuzione / Benefits
Competitive base salary and performance related incentives
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 preparation and review of study documentation, including protocols and clinical study reports
Requisiti fondamentali
Bachelor's degree in scientific or healthcare-related field
Minimum of 2 years of experience as a Clinical Research Associate
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
Willingness to travel as required (approximately 60%)
Strong organizational skills
Clear communication
Attention to detail
ICH-GCP knowledge
Clinical trial monitoring
Data review and query resolution

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