At ICON Strategic Solutions, the Clinical Research Associate works in a sponsor-dedicated model, supported by ICON’s global expertise. The CRA I contributes to clinical trial operations and collaborates with the team to deliver high-quality outcomes across clinical programs. The client is seeking candidates with experience monitoring Ophthalmology trials or across multiple therapeutic areas. The role involves coordinating study setup and monitoring, maintaining study documentation and status reports, supporting study documentation and feasibility work, and collaborating with stakeholders, investigators, and site staff while ensuring patient safety and compliance.
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Job Type
Full-time
Career Level
Entry Level