Drive clinical excellence at Worldwide Clinical Trials as a Senior Clinical Research Associate. This position is key to managing oncological research sites and ensuring compliance with regulations.

You will leverage your five-plus years of CRA experience to oversee research activities across clinical trial sites. Your role will involve site selection, data training, and compliance checks during the study lifecycle. Your commitment to quality in clinical operations will directly affect patient outcomes in various disease areas.

Key Responsibilities:
• Oversee research activities at participating clinical sites
• Conduct study initiation visits for compliance assurance
• Train site personnel on data collection processes




• Manage budgets and negotiate site contracts
• Ensure proper closure of research sites after studies

Requirements:
• 5+ years as a Clinical Research Associate required
• Bachelor’s or Nursing degree essential
• Experience in Oncology required
• Fluent in both English and French
• Must reside in Canada and have the ability to travel

Utilize your communication and organizational skills to support impactful clinical research with Worldwide Clinical Trials.
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📌 Senior Clinical Research Associate Canada (Quebec City)
🏢 Worldwide Clinical Trials
📍 Quebec City