Clinical Research Coordinator

Responsibilities

• Coordinate clinical research protocols for the Michael Cuccione Childhood Cancer Research Program, focusing on precision oncology for pediatric cancer and blood disorders.
• Identify and track potential patients, reviewing and confirming eligibility based on specific protocol criteria.
• Retrieve, interpret, and abstract complex data from health records, including reporting follow-up data on participants.
• Manage biological sample handling and shipment in adherence to study protocols.
• Prepare for and assist with audit and monitoring visits, including identifying source documents and creating responses to reports.
• Ensure accurate and timely data capture into electronic systems and maintain organized study files and databases.
• Act as a liaison between healthcare and interdisciplinary teams to facilitate project management and information exchange.
• Maintain study procedure documents and perform data queries to ensure research integrity.

Requirements

• University degree in a relevant discipline or completion of a relevant technical program.
• Minimum of three years of related experience in a clinical research setting.
• Strong knowledge of Good Clinical Practice (GCP).
• Proficiency in Microsoft Office (Word, Excel, and Access).
• Solid understanding of medical terminology.
• Demonstrated commitment to equity, diversity, and inclusion.

Preferred Qualifications

• Clinical research professional certification through SoCRA or ACRP.
• Transportation of Dangerous Goods (TDG) Certificate.
• Demonstrated experience or knowledge in pediatric oncology.
• Ability to work effectively under pressure and meet strict deadlines.

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 fostering an inclusive and diverse community that supports inspired students, faculty, and staff in their journey of discovery.