CRA II
ICON
Clinical Research Associate II position at ICON in the Toronto area, supporting sponsor-dedicated clinical trial programs. The role involves site qualification, initiation, monitoring, and closeout activities with emphasis on protocol compliance, GCP adherence, and participant protection oversight.
Responsibilities
- Perform site qualification, initiation, monitoring, and closeout activities as assigned
- Verify protocol, GCP, and regulatory compliance; ensure participant protection
- Review source data, essential documents, and site processes for accuracy and completeness
- Identify findings and risks; develop and follow up on corrective actions
- Maintain clear communication with investigators, site staff, and study teams
Requirements
- Life sciences, healthcare, or clinical research qualification or equivalent experience
- Minimum 2 years experience as a Clinical Research Associate
- In-depth knowledge of ICH GCP guidelines and clinical trial regulations
- Practical site monitoring and site management experience
- Experience with site qualification, initiation, monitoring and closeout activities
- Ability to verify protocol compliance and participant protection measures
Vacancy posted 17 hours ago
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