Clinical Research Associate for Oncology Trials
Prevail InfoWorks • toronto, Canada
Role Description
Advance your career with Prevail as a Clinical Research Associate specializing in oncology trials in Canada. This role integrates your skills in site monitoring and trial management for Breast Cancer studies.
As a Clinical Research Associate, you will perform monitoring activities for Phase I-IV trials while working remotely or on-site across British Columbia, Ontario, and Quebec. Your responsibilities will include managing site compliance with ICH-GCP guidelines and industry standards. You can apply your judgment to elevate site performance and tackle issues effectively.
Key Responsibilities:
• Conduct interim monitoring and site close-out visits
• Verify informed consent has been obtained
• Document all activities in compliance with SOPs
• Ensure safety and integrity of clinical data
• Facilitate investigator meetings and training sessions
Requirements:
• Strong knowledge of GCP and regulatory requirements
• Excellent skills in Word, Excel, and presentat...
As a Clinical Research Associate, you will perform monitoring activities for Phase I-IV trials while working remotely or on-site across British Columbia, Ontario, and Quebec. Your responsibilities will include managing site compliance with ICH-GCP guidelines and industry standards. You can apply your judgment to elevate site performance and tackle issues effectively.
Key Responsibilities:
• Conduct interim monitoring and site close-out visits
• Verify informed consent has been obtained
• Document all activities in compliance with SOPs
• Ensure safety and integrity of clinical data
• Facilitate investigator meetings and training sessions
Requirements:
• Strong knowledge of GCP and regulatory requirements
• Excellent skills in Word, Excel, and presentat...