Clinical Research Coordinator I
Core
Coordinate clinical studies for the Home Hemodialysis program, managing patient recruitment, data collection, and regulatory compliance for University Health Network and external sponsors.
Role type
Clinical Research Coordinator I
Builds
Clinical research studies and data integrity for home dialysis programs
Domain
Healthcare / Nephrology / Clinical Trials
Deliverable
client delivery
Required skills
Clinical study coordination, patient recruitment, informed consent processes, data management, safety monitoring, regulatory compliance (ICH-GCP, PHIPA, Health Canada/FDA), budgeting, contract review, tool development for data collection
Preferred skills
Independent judgement, team leadership, study feasibility review
Technologies
None explicitly stated
Responsibilities
Coordinate clinical studies including screening, recruitment, and informed consent; execute study visits and assessments; collect and process samples; manage data and monitor safety; assist with study audits; ensure compliance with ICH-GCP and local regulations; contribute to study feasibility reviews; submit studies for REB review; develop data collection tools
Seniority
Individual Contributor, minimal direction required