Elevate your career as a Senior Clinical Research Associate in Quebec City with expertise in clinical monitoring and compliance. Ensure regulatory adherence while managing site performances and patient safety.

This position entails conducting site qualifications, monitoring compliance with ICH-GCP, and managing clinical trial activities—either on-site or remotely. The Senior CRA will verify informed consent and attend to patient confidentiality, ensuring data integrity throughout the trial process.

Key Responsibilities:
• Perform site qualification and initiation visits
• Conduct interim monitoring and close-out evaluations
• Manage documentation and communication logs
• Oversee site compliance with GCP and regulatory standards
• Ensure accurate clinical data entry and query resolution

Requirements:
• Bachelor’s degree or RN in a relevant field
• Proficient knowledge of GCP/ICH Guidelines
• Strong co...