Found Description
Drive essential clinical research initiatives as a Lead Clinical Research Coordinator IV at McMaster University's Juravinski Cancer Centre, utilizing your regulatory expertise in a hybrid work setup.
In this critical role, you will serve as the main regulatory resource for clinical trials, engaging with Health Canada and managing the Ontario Cancer Research Ethics Board applications. Your six years of relevant experience, including supervisory responsibility, will ensure efficient management of multiple clinical research projects. You'll be vital in developing quality assurance measures and educational resources while coordinating communication across various stakeholders.
Key Responsibilities:
• Oversee clinical trial regulatory submissions and compliance
• Develop strategic plans for multi-site clinical trials
• Implement quality assurance and inspection readiness plans
• Lead data collection efforts and ensure accurate reporting
• Conduct meetings with internal ...
In this critical role, you will serve as the main regulatory resource for clinical trials, engaging with Health Canada and managing the Ontario Cancer Research Ethics Board applications. Your six years of relevant experience, including supervisory responsibility, will ensure efficient management of multiple clinical research projects. You'll be vital in developing quality assurance measures and educational resources while coordinating communication across various stakeholders.
Key Responsibilities:
• Oversee clinical trial regulatory submissions and compliance
• Develop strategic plans for multi-site clinical trials
• Implement quality assurance and inspection readiness plans
• Lead data collection efforts and ensure accurate reporting
• Conduct meetings with internal ...
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