Clinical Research Coordinator III (Phase 1)

Responsibilities

• Recruit study participants through identification, screening, and obtaining informed consent
• Coordinate patient visit schedules according to study protocols
• Execute study visit aspects including adverse event assessment, safety monitoring, and medication administration
• Collect, process, and ship samples according to clinical protocols
• Provide clinical care and implement data collection and source documentation per UHN policy and ICH/GCP guidelines

Requirements

• Bachelor's degree or recognized equivalent
• Current registration with the College of Nurses of Ontario
• Minimum 3 to 5 years of clinical or professional experience
• Registered Nurse designation with at least 3 years of experience
• Strong knowledge of Phase I Clinical Trials
• Proficiency with MS Office software

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

About the Company

UHN is Canada’s #1 hospital and the world’s #1 publicly funded hospital. As Canada's top research hospital, UHN is a national and international source for discovery, education, and patient care, with major research in neurosciences, cardiology, oncology, and genomic medicine.