Join our team as a Clinical Research Coordinator to oversee clinical studies in compliance with regulatory standards. This on-site role requires strong organizational and communication skills to manage all aspects of research effectively.
As a Clinical Research Coordinator, you will play a vital role in the coordination and execution of clinical research studies. You will ensure adherence to Good Clinical Practice, oversee participant recruitment, and manage documentation essential for integrity. Your proficiency in electronic data systems will support accurate data management and regulatory compliance.
Key Responsibilities:
• Coordinate participant recruitment and informed consent processes
• Ensure compliance with Health Canada and IRB standards
• Accurately collect and enter data into EDC systems
• Maintain comprehensive study documentation and regulatory binders
• Monitor and report adverse events adhering to protocols
Requirements:
• Bachelor’s degree in...