OverviewIn this CRA II role, you monitor and support clinical trials within ICON's sponsor-dedicated model, applying global expertise to ensure data quality and patient safety.
You work with investigators and site staff to drive compliant study conduct and timely documentation.
The position blends independent work with cross-functional collaboration in a fast-paced environment.
You'll contribute to trials that advance new treatments for patients and agevolazioni from a structured development path.
Retribuzione / BenefitsCompetitive base salary
Health and wellbeing programmes
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities
ResponsabilitàConduct site qualification, initiation, monitoring, and close-out visits
Ensure protocol compliance, data integrity, and patient safety throughout the trial




Collaborate with investigators and site staff to facilitate 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 CSRs
Requisiti fondamentaliBachelor's degree in a 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 approximately 60%
strong communication
attention to detail
self-motivation and independence
clinical trial processes
ICH-GCP guidelines
data review and query resolution

📌 Clinical Research Associate (Varese)
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📍 Varese