Job Description
Join Prevail as a Clinical Research Associate specializing in oncology studies. This role focuses on monitoring and site management for clinical research projects across Canada, particularly for Breast Cancer.
As a seasoned CRA, you will conduct Phase I-IV clinical studies, ensuring compliance with protocols, SOPs, and regulatory requirements. Your responsibilities will include site monitoring, data integrity assessments, and providing crucial support for patient recruitment and retention. Collaborate with project teams and maintain a strong knowledge base of ICH and GCP guidelines.
Key Responsibilities:
• Perform site qualification and initiation for clinical studies
• Conduct interim monitoring and close-out visits
• Evaluate site performance and develop action plans
• Verify informed consent processes for subjects
• Document activities in compliance with SOPs
Requirements:
• Experience in clinical research monitoring
• Knowledge of ICH/GCP guidelines
As a seasoned CRA, you will conduct Phase I-IV clinical studies, ensuring compliance with protocols, SOPs, and regulatory requirements. Your responsibilities will include site monitoring, data integrity assessments, and providing crucial support for patient recruitment and retention. Collaborate with project teams and maintain a strong knowledge base of ICH and GCP guidelines.
Key Responsibilities:
• Perform site qualification and initiation for clinical studies
• Conduct interim monitoring and close-out visits
• Evaluate site performance and develop action plans
• Verify informed consent processes for subjects
• Document activities in compliance with SOPs
Requirements:
• Experience in clinical research monitoring
• Knowledge of ICH/GCP guidelines
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