Experienced Clinical Research Associate for Oncology Trials (Quebec City)

Experienced Clinical Research Associate for Oncology Trials (Quebec City)

17 Apr
|
Parexel International
|
Quebec City

17 Apr

Parexel International

Quebec City

Elevate your career as a Clinical Research Associate with a focus on oncology studies. This role includes overseeing site management and compliance while ensuring outstanding study outcomes in a remote or on-site setting.
In this senior CRA position, you will engage closely with investigators and study teams. Your responsibilities will include site selection, training site staff, and maintaining compliance with ICH-GCP guidelines. Contribute to the success of critical oncology and cell therapy trials by ensuring that all study processes run smoothly and efficiently.
Key Responsibilities:
• Select and qualify investigators for trials
• Train and support site staff in study-related tasks
• Monitor study sites for compliance with guidelines




• Conduct remote and on-site visit monitoring
• Ensure accurate documentation and reporting
Requirements:
• Robust background in oncology clinical trials
• Bachelor's degree in a relevant field
• Knowledge of ICH-GCP and local regulations
• Strong communication and collaboration skills
• Ability to manage multiple priorities effectively
Leverage your oncology expertise and transform clinical trial management, enhancing outcomes across critical studies.
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📌 Experienced Clinical Research Associate for Oncology Trials (Quebec City)
🏢 Parexel International
📍 Quebec City

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