Opportunity Description
Join us as a Clinical Research Associate specializing in oncology studies. This role focuses on managing Phase I-IV trials and is available for qualified candidates across Canada.
We seek an experienced Clinical Research Associate with expertise in Breast Cancer studies. In this versatile contract position, you will manage site performance and regulatory compliance, whether working on-site or remotely. Your role is vital in ensuring informed consent and elevated site operations throughout the study timeline.
Key Responsibilities:
• Carry out site qualification, initiation, and close-out visits
• Monitor site performance and tackle issues responsively
• Ensure compliance with informed consent processes
• Maintain regulatory adherence during site operations
• Review documentation for quality control and completeness
Requirements:
• Familiarity with ICH/GCP compliance standards
• Strong communication and interpersonal skills
• Ability to travel up to 65%
We seek an experienced Clinical Research Associate with expertise in Breast Cancer studies. In this versatile contract position, you will manage site performance and regulatory compliance, whether working on-site or remotely. Your role is vital in ensuring informed consent and elevated site operations throughout the study timeline.
Key Responsibilities:
• Carry out site qualification, initiation, and close-out visits
• Monitor site performance and tackle issues responsively
• Ensure compliance with informed consent processes
• Maintain regulatory adherence during site operations
• Review documentation for quality control and completeness
Requirements:
• Familiarity with ICH/GCP compliance standards
• Strong communication and interpersonal skills
• Ability to travel up to 65%
Interested in this opportunity? Apply now through Expertini.
Apply for this Position