At ICON Strategic Solutions, the Clinical Research Associate works in a sponsor-dedicated model supported by ICON’s global expertise. The role contributes to clinical trial monitoring activities and is responsible for assigned deliverables while working collaboratively. It involves conducting site visits, ensuring protocol compliance and data integrity, supporting investigators and site staff, reviewing clinical data, and contributing to study documentation. The role requires approximately 60% travel. ICON describes its environment as offering stability, career development, and collaboration, with work contributing to treatments that benefit patients worldwide.
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Job Type
Full-time
Career Level
Mid Level