At ICON Strategic Solutions, the Clinical Research Associate II works in a sponsor-dedicated model supported by ICON’s global expertise. The role contributes to clinical trial monitoring and the development of treatments for patients worldwide. The CRA II is responsible for assigned deliverables and collaborates with investigators, site staff, and colleagues to support smooth study conduct. The position is based in California and requires approximately 60% travel. The role involves conducting site qualification, initiation, monitoring, and close-out visits; ensuring protocol compliance, data integrity, and patient safety; reviewing data and resolving queries; and contributing to the preparation and review of study documentation, including protocols and clinical study reports.
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Job Type
Full-time
Career Level
Mid Level