Support innovative research projects as a Clinical Research Coordinator. Take charge of study activities, ensure protocol adherence, and maintain participant data confidentiality.
In this role, you will coordinate diverse clinical trials while effectively managing participant interactions and data collection processes. Your contributions will extend to supporting regulatory submissions and maintaining operational compliance across studies. Strong analytical and organizational skills are essential to thrive in this independent yet team-oriented position.
Key Responsibilities:
• Coordinate multi-project clinical research activities
• Ensure accurate collection and management of clinical data
• Supervise and train research assistants on protocols
• Collaborate with healthcare team members systematically
• Prepare for regulatory meetings and documentation requirements
Requirements:
• Degree in a relevant discipline or significant experience
• Minimum 3 years in a clinical research setting
• Understanding of ICH/GCP methodologies is an asset
• Strong attention to detail and critical thinking skills
• Availability for flexible working hours as needed
Leverage your clinical research expertise to enhance study outcomes and maintain integrity within innovative healthcare environments.
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Apply on Kit Job: kitjob.ca/job/2fslxf
📌 Clinical Research Coordinator Focusing on Protocol Execution and Data Integrity (Vancouver)
🏢 The University of British Columbia
📍 Vancouver
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