As a CRA II at ICON, you design and analyze clinical trials, ensuring data integrity and patient safety while advancing innovative therapies. You will monitor sites, collaborate with investigators, and contribute to study documentation. This role supports cross-functional teams in a fast-paced, global environment and involves travel. You will help bring new medicines to patients faster by upholding high-quality standards and regulatory compliance.
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
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
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 communication
Knowledge of clinical trial processes and ICH-GCP
Data review and query resolution
Regulatory compliance understanding
Clinical Research Associate varese, lombardia, it
📌 Clinical Research Associate (Varese)
🏢 Altro
📍 Varese