Clinical Study and Regulatory Specialist I

**Clinical Study and Regulatory Specialist I at University Health Network in Toronto, Canada** **What you'll do** - Prepare Health Canada and Research Ethics Board submissions - Monitor and ensure quality and integrity of clinical trial data - Coordinate and monitor data according to trial protocols - Complete documentation following ICH-GCP and FDA standards **What they're looking for** - Experience in clinical trial coordination and regulatory submissions - Knowledge of ICH-GCP, FDA and federal code standards - Ability to maintain accurate and timely clinical trial documentation - Understanding of data quality and integrity requirements **Details** - Location: Toronto, Canada - Type: Full-time - Salary: null