Contract Clinical Research Associate Oncology

Explore an exciting contract as a Clinical Research Associate focused on Oncology within Canada. Your expertise in Breast Cancer studies will ensure compliant and effective project monitoring at clinical sites.
In this essential role, you will oversee Phase I-IV clinical projects, managing site activities both on-site and remotely while adhering to protocols, ICH-GCP, and regulatory standards. Your judgment will help evaluate site performance, support patient recruitment, and maintain data integrity. Experience with both site qualification and close-out processes is a plus while working with diverse study teams.
Key Responsibilities:
• Conduct site qualification, initiation, and monitoring visits
• Ensure compliance with ICH-GCP and local regulations
• Evaluate site performance and escalate issues promptly
• Maintain accurate project documentation and tracking
• Manage investigator site files and trial master files
Requirements:
• Bachelor’s degree in a healt...