Elevate your career as a Clinical Monitoring Associate specializing in oncology. This role focuses on regulatory compliance and monitoring for clinical trials, ensuring data integrity in phase 1 studies.
The position requires a robust understanding of therapeutic areas, especially oncology. You will perform regulatory document reviews, monitor adherence to processes, and conduct site visits, adhering to all legal and protocol guidelines. Your expertise will be crucial in retraining site staff, document verification, and facilitating site payments to ensure smooth trial operations.
Key Responsibilities:
• Conduct monitoring and co-monitoring for clinical trials
• Review regulatory documents accurately for compliance
• Identify and document site findings, implementing corrective actions




• Ensure precision in study documents and data integrity
• Facilitate investigator site payments and tracking
Requirements:
• Background in oncology and phase 1 clinical studies
• Solid knowledge of regulatory processes and compliance
• Experience in writing clinical monitoring plans
• Ability to collaborate effectively with study teams
• Skills in preparing site visit reports and documentation
Utilize your clinical expertise and regulatory knowledge to support impactful oncology studies as a Clinical Monitoring Associate.
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📌 Clinical Monitoring Associate in Oncology (Toronto)
🏢 Mason Group
📍 Toronto