Found Description
Join ICON plc as a Clinical Research Associate focused on oncology in Vancouver. Leverage your skills in monitoring clinical trials and ensuring regulatory compliance within a vibrant team environment.
In this senior position, you will oversee site performance and maintain high standards of patient safety. A minimum of three years' relevant experience in the pharmaceutical or CRO industry is essential. You will manage site interactions, documentation, and support study activities that drive patient engagement.
Key Responsibilities:
• Facilitate all phases of site visits from selection to close-out
• Maintain compliance with industry regulations and guidelines
• Document site progress and manage site training records
• Monitor patient safety and ensure timely reporting
• Collaborate with cross-functional team members effectively
Requirements:
• 3+ years of relevant on-site clinical monitoring experience
• Bachelor’s in Life Sciences or an equivalent qualifi...
In this senior position, you will oversee site performance and maintain high standards of patient safety. A minimum of three years' relevant experience in the pharmaceutical or CRO industry is essential. You will manage site interactions, documentation, and support study activities that drive patient engagement.
Key Responsibilities:
• Facilitate all phases of site visits from selection to close-out
• Maintain compliance with industry regulations and guidelines
• Document site progress and manage site training records
• Monitor patient safety and ensure timely reporting
• Collaborate with cross-functional team members effectively
Requirements:
• 3+ years of relevant on-site clinical monitoring experience
• Bachelor’s in Life Sciences or an equivalent qualifi...
Ready to Apply?
Submit your application for Clinical Research Associate - Oncology Focus at ICON Clinical Research
Apply Now