Clinical Research Coordinator

Responsibilities

• Coordinate clinical research protocols, including Phase I, II, and III chemotherapy and hematology studies
• Identify potential study participants and review eligibility criteria
• Manage patient registration and ensure accurate completion of electronic and paper data capture forms
• Create study-specific consents, assents, and required regulatory documentation
• Procure, safely ship, and maintain documentation for study specimens according to federal regulations
• Submit ethics applications, amendments, and study closures via the RISe database
• Act as a liaison between the healthcare team and laboratory teams for project management
• Prepare for and participate in audits and study monitoring visits from regulatory bodies

Requirements

• University degree in a relevant discipline or completion of a relevant technical program
• Minimum of three years of related research experience
• Strong knowledge of medical terminology and patient record systems
• Proficiency in Microsoft Office (Word, Excel, and Access)
• Knowledge of Good Clinical Practice (GCP)
• Commitment to equity, diversity, and inclusion in the workplace

Preferred Qualifications

• Clinical research professional certification (SoCRA or ACRP)
• Transportation of Dangerous Goods Certificate
• Experience in pediatric oncology or hematology
• Familiarity with database management programs

About the Company

The University of British Columbia is a global centre for research and teaching, consistently ranked among the top 20 public universities globally. We are committed to attracting and sustaining a diverse workforce to drive excellence in research, innovation, and learning.