Job Description
Elevate your career as a Clinical Research Associate focused on Oncology, working remotely or on-site across Canada. This role demands expertise in Breast Cancer studies, ensuring compliance and project success.
Join a dynamic team where you’ll perform monitoring and management for Phase I-IV clinical studies. As a seasoned CRA, you’ll oversee site activities, maintain ICH-GCP compliance, and ensure patient confidentiality throughout the study lifecycle. Your experience will be vital in fostering collaboration and effective communication with site personnel.
Key Responsibilities:
• Perform site qualification, initiation, and monitoring tasks
• Evaluate site performance and develop action plans
• Verify informed consent processes for each subject
• Maintain accuracy of the Investigator Site File
• Manage site-level communication and project timelines
Requirements:
• Strong knowledge of ICH/GCP Guidelines
• Excellent communication and interpersonal skills
Join a dynamic team where you’ll perform monitoring and management for Phase I-IV clinical studies. As a seasoned CRA, you’ll oversee site activities, maintain ICH-GCP compliance, and ensure patient confidentiality throughout the study lifecycle. Your experience will be vital in fostering collaboration and effective communication with site personnel.
Key Responsibilities:
• Perform site qualification, initiation, and monitoring tasks
• Evaluate site performance and develop action plans
• Verify informed consent processes for each subject
• Maintain accuracy of the Investigator Site File
• Manage site-level communication and project timelines
Requirements:
• Strong knowledge of ICH/GCP Guidelines
• Excellent communication and interpersonal skills
Ready to Apply?
Submit your application today and join our talented team at Prevail InfoWorks.
Submit ApplicationJob Details
- Location kamloops, thompson nicola regional district
- Job Type Full-time
- Category Other-General
- Posted Date June 05, 2026
- Application Deadline July 15, 2026