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About the Role
Accelerate your clinical research career as a Clinical Research Associate II at ICON in Calgary, Alberta. Play a crucial role in monitoring and analyzing clinical trials.
In this role, you will oversee clinical trial monitoring, ensuring high-quality data and patient safety. As a CRA II, your responsibilities include site qualification and maintaining compliance with regulatory standards. Collaborating with investigators, you will contribute to the advancement of innovative treatments through meticulous data analysis and documentation preparation.
Key Responsibilities:
• Conduct initiation, monitoring, and close-out visits
• Ensure adherence to protocols and safeguard patient safety
• Collaborate with site staff for smooth operations
• Review and resolve data queries efficiently
• Prepare clinical study documentation and reports
Requirements:
• Bachelor’s in a scientific discipline
• Minimum 2 years as a Clinical Research Associate
• Knowledge of ICH-GC...
In this role, you will oversee clinical trial monitoring, ensuring high-quality data and patient safety. As a CRA II, your responsibilities include site qualification and maintaining compliance with regulatory standards. Collaborating with investigators, you will contribute to the advancement of innovative treatments through meticulous data analysis and documentation preparation.
Key Responsibilities:
• Conduct initiation, monitoring, and close-out visits
• Ensure adherence to protocols and safeguard patient safety
• Collaborate with site staff for smooth operations
• Review and resolve data queries efficiently
• Prepare clinical study documentation and reports
Requirements:
• Bachelor’s in a scientific discipline
• Minimum 2 years as a Clinical Research Associate
• Knowledge of ICH-GC...
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