Clinical Research Coordinator III (Phase 1)

Responsibilities

• Recruit study participants by identifying and screening potential subjects and obtaining informed consent
• Coordinate patient visit schedules according to study protocols
• Execute all aspects of study visits, including monitoring safety, assessing adverse events, and administering treatments
• Perform clinical tasks such as vital signs, ECGs, and sample collection, processing, and shipment
• Provide clinical care for trial participants and manage data collection and source documentation in accordance with UHN policy and ICH/GCP guidelines

Requirements

• Bachelor's degree or recognized equivalent
• Current registration with the College of Nurses of Ontario (CNO)
• Registered Nurse (RN) designation with at least 3 years of experience
• 3 to 5 years of clinical or professional experience
• Strong knowledge base in Phase I Clinical Trials
• Excellent organizational, time management, and analytical skills
• Proficiency in MS Office (Word, Excel, PowerPoint)

Preferred Qualifications

• Recognized certification in clinical research (ACRP or SOCRA)
• Chemotherapy certification (deSouza Institute)
• Training in ICH/GCP guidelines
• Knowledge of IATA shipping regulations and basic laboratory procedures

Benefits

• Competitive salary package ($84,779 - $105,968 per year)
• Membership in the Healthcare of Ontario Pension Plan (HOOPP)
• Flexible work environment and opportunities for professional development
• Access to transit and UHN shuttle services
• Various corporate discounts including travel, restaurants, and parking

About the Company

University Health Network (UHN) is Canada’s #1 hospital and a global leader in publicly funded healthcare. As a top research hospital affiliated with the University of Toronto, UHN operates multiple sites, including the Princess Margaret Cancer Centre. We are dedicated to building a healthier world through groundbreaking biomedical research, education, and world-class patient care.