Clinical Research Associate (CRA II) - prior monitoring experience needed
About this role
About the Role ICON is seeking a Clinical Research Associate II (CRA II) with prior monitoring experience to support the design, analysis, and oversight of clinical trials. You will contribute to advancing innovative treatments while ensuring patient safety and high-quality data across trial sites. What You'll Do
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborate with investigators and site staff to facilitate smooth study conduct.
- Perform data review and resolution of queries to maintain high-quality clinical data.
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports. What We're Looking For
- Bachelor's degree in a scientific or healthcare-related field.
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