CRA II (Clinical Research Associate II)
About this role
Job title: CRA II (Clinical Research Associate II)
About the Role As a CRA II at ICON, you will contribute to clinical trial operations, delivering high-quality monitoring across our programmes. You will work with your team and stakeholders to coordinate activities for study setup and monitoring, maintain study documentation, and support cost efficiency while ensuring patient safety and regulatory compliance.
What You'll Do
- Deliver clinical trial monitoring work to a high standard, working closely with your team and stakeholders.
- Coordinate all activities for setting up and monitoring a study, complete accurate study status reports, and maintain study documentation.
- Run sponsor-generated queries efficiently and participate in preparation and review of study documentation and feasibility studies for new proposals.
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