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Clinical Research Associate – Oncology Expertise
Job in
Quebec, Québec, Province de Québec, Canada
Listed on 2026-06-10
Listing for:
Worldwide Clinical Trials Canada Limited
Full Time
position Listed on 2026-06-10
Job specializations:
-
Research/Development
Clinical Research -
Healthcare
Clinical Research
Job Description & How to Apply Below
Join Worldwide as a Senior Clinical Research Associate specializing in Oncology. Lead research activities, maintain site compliance, and support clinical study management.
This position involves overseeing various clinical research projects, with a focus on site management in Oncology. You will conduct initiation visits, ensure adherence to regulatory standards, and train sites on crucial data collection procedures. Strong communication and organizational skills are vital to excel in this role.
Key Responsibilities:
• Direct site management and activity coordination
• Perform study initiation visits (SIVs) effectively
• Ensure compliance in informed consent and safety reporting
• Assist with contracts and budget negotiations
• Guide sites on proper data reporting and collection
Requirements:
• Minimum 5 years of experience in a Clinical Research Associate role
• Oncology background required
• University degree or Nursing degree needed
• Expertise in Microsoft Office and clinical systems
• Fluency in both English and French, with residency in Canada
Leverage your oncology expertise and project management skills to enhance Worldwide's clinical research efforts.
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Position Requirements
10+ Years
work experience
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