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About the Role
Join our dynamic Full Service Outsourcing team as a CRA focused on CAR-T oncology projects. We are seeking skilled candidates on Canada's East and West Coasts with experience in clinical monitoring.
As a CRA, you will ensure compliance with protocols and high-quality data collection in clinical trials. Key tasks include site management, monitoring study protocols, and liaising with project vendors. French-speaking candidates will be given priority. Adaptability and teamwork are crucial due to the fast-paced nature of our work environment.
Key Responsibilities:
• Manage all aspects of site monitoring and data integrity
• Confirm adherence to informed consent and regulatory requirements
• Conduct Serious Adverse Event reporting and follow-up
• Facilitate training for new team members and projects
• Handle study file maintenance and perform feasibility work
Requirements:
• University degree or allied health certification
• 1 - 3+ years of Clinical Monitoring ...
As a CRA, you will ensure compliance with protocols and high-quality data collection in clinical trials. Key tasks include site management, monitoring study protocols, and liaising with project vendors. French-speaking candidates will be given priority. Adaptability and teamwork are crucial due to the fast-paced nature of our work environment.
Key Responsibilities:
• Manage all aspects of site monitoring and data integrity
• Confirm adherence to informed consent and regulatory requirements
• Conduct Serious Adverse Event reporting and follow-up
• Facilitate training for new team members and projects
• Handle study file maintenance and perform feasibility work
Requirements:
• University degree or allied health certification
• 1 - 3+ years of Clinical Monitoring ...
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