Research Coordinator (Clinical Trials)

About the role

The University of British Columbia's Department of Ophthalmology is seeking a Research Coordinator to support clinical trial activities over a two‑year fixed‑term appointment. The role involves managing all aspects of trial conduct, from ethics submissions to participant recruitment and data documentation, ensuring compliance with Good Clinical Practice standards.

Key responsibilities

• Prepare and submit interim Clinical Research Ethics Board applications.
• Coordinate study project timelines, participant recruitment, and visit scheduling.
• Conduct study visits, complete case record forms, and maintain accurate trial documentation.
• Manage study drug accountability and oversee study file organization.
• Collaborate with clinical departments, laboratory services, and external pharmaceutical partners.

Required profile

• Strong organizational and communication abilities.
• High motivation, enthusiasm, and initiative for managing research trials.
• Experience working in a clinical or research environment is preferred.

Required skills

• Good Clinical Practice (GCP) knowledge.
• Clinical trial management.
• Case record form (CRF) management.

What we offer

• Opportunity to work within a leading academic ophthalmology department.
• Exposure to multidisciplinary clinical research teams.
• Professional development in clinical trial coordination.