Experienced Clinical Research Coordinator Role (Hamilton)

Lead clinical trials as a Clinical Research Coordinator IV at McMaster University. This role requires regulatory expertise and strong project management skills in a hybrid setting. The TRACE Unit at McMaster’s Faculty of Health Sciences is seeking a dedicated professional with a Master's degree and substantial experience in clinical research. You will manage trials, ensuring compliance with Health Canada regulations while leading stakeholder communication. Your ability to adapt and coordinate will directly influence the success of multiple clinical projects. Key Responsibilities: - Facilitate the development of trial protocols - Coordinate and track trial timelines effectively - Serve as liaison for regulatory applications - Implement quality assurance and manage inspections - Organize data collection and address regulatory challenges Requirements: - Master’s degree in a relevant discipline - Minimum 6 years of experience with supervisory duties - Excellent communication and organizational skills - Familiarity with electronic data systems - Hybrid work model: in office 2 days per week Apply your regulatory and management proficiency to drive impactful research at McMaster. Apply on Kit Job: kitjob.ca/job/2pdx0z