Elevate clinical research at Worldwide Clinical Trials as a bilingual Clinical Research Associate. Leverage your expertise in Oncology and manage diverse clinical study activities across Canada.

In this senior position, you will oversee research activities at various sites while supporting regulatory compliance and safety reporting. With extensive interaction in the Oncology field, your role will encompass study initiation, budget negotiation, and site training. You will collaborate with a committed team and receive opportunities for skilled growth toward Clinical Trial Manager roles.

Key Responsibilities:
• Manage clinical research activities at participating sites
• Conduct study initiation visits (SIVs) effectively




• Ensure compliance with informed consent and safety reporting
• Negotiate contracts and budgets with sites
• Train sites on data collection and reporting protocols

Requirements:
• 5+ years as a Clinical Research Associate
• 4-year degree or Nursing Degree required
• Oncology experience is mandatory
• Fluent in English and French, both written and spoken
• Willingness to travel regionally for site visits

Drive impactful clinical research and make a difference in patients' lives with Worldwide Clinical Trials.
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📌 Bilingual Clinical Research Associate Canada (Quebec City)
🏢 Worldwide Clinical Trials Holdings
📍 Quebec City