ICON seeks a Clinical Research Associate II to design and analyze clinical trials, interpreting medical data while ensuring protocol compliance and data integrity. The role involves site monitoring, investigator collaboration, and documentation review to support innovative treatment advancement.
Responsibilities
Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
Ensure protocol compliance, data integrity, and patient safety throughout trial process
Collaborate with investigators and site staff to facilitate smooth study conduct
Perform data review and resolve queries to maintain high-quality clinical data
Contribute to preparation and review of study documentation including protocols and reports
Requirements
Bachelor's degree in scientific or healthcare-related field
Minimum 2 years of clinical trial monitoring experience as a CRA
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 fast-paced environment
Willingness to travel approximately 60% as required
Compensation:
€40,944–€51,180 base

📌 Clinical Research Associate (Milano)
🏢 Icon
📍 Milano