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Job Description & How to Apply Below
As a full-time Clinical Research Coordinator, you will execute vital research activities for various clinical trials at the Centre. You’ll collaborate closely with physicians and nurses to meet rigorous ethical standards and ensure successful study milestones. The role also includes supervising research assistants to facilitate project management.
Key Responsibilities:
• Supervise daily activities of clinical research projects
• Enroll participants and collect biological samples
• Maintain project timelines and communication with staff
• Ensure compliance with ethical and regulatory guidelines
• Execute preliminary data analysis and documentation
Requirements:
• Bachelor’s degree or equivalent in a relevant field
• At least three years of clinical research experience
• Experience with ICH/GCP guidelines
• Excellent communication and organizational skills
• Ability to work independently and manage multiple tasks
Contribute to impactful research that enhances patient care and innovation at UBC.
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