Take on a pivotal role as a Clinical Research Associate for oncology projects with Prevail. This contract position supervises Phase I-IV studies focusing on Breast Cancer while managing site progress and compliance.
As an experienced Clinical Research Associate based in Canada, specifically in BC, Ontario, or Quebec, you will independently conduct monitoring activities and oversee site management tasks. Your expertise is essential in ensuring regulatory compliance, managing site staff performance, and maintaining data integrity during clinical trials.
Key Responsibilities:
• Perform site qualification, initiation and monitoring
• Evaluate site performance and escalate serious issues
• Verify informed consent has been obtained and documented
• Maintain investigator site files and ensure compliance
• Support patient recruitment and retention strategies
Requirements:
• Experience with ICH/GCP Guidelines and regulatory requirements
• Strong interpersonal and c...