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Job Description & How to Apply Below
Elevate clinical trial excellence as a Clinical Research Coordinator I at Niagara Health. This full-time role involves coordinating trials, recruiting patients, and ensuring compliance across multiple sites.
Pursue a temporary full-time position with the Niagara Health Knowledge Institute. You will utilize your specialized knowledge to manage clinical trials and observational studies, reporting directly to the Director of Research Operations. Responsibilities include overseeing patient visits, data collection, and managing compliance while engaging with diverse collaborators.
Key Responsibilities:
• Coordinate initiation and administration of clinical trials
• Conduct patient visits and offer oversight for Research Visitors
• Manage clinical trial compliance with regulatory requirements
• Conduct data entry and monitor trial conduct
• Screen and recruit participants effectively
Requirements:
• Bachelor’s degree in health-related field
• 3 years of experience in clinical research settings
• Certification in ICH GCP, Health Canada guidelines
• Experience with electronic patient records and REDCap
• Strong organizational and communication skills
Utilize your expertise in clinical research to contribute to advancing healthcare at Niagara Health.
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