Research Coordinator

This position has a term length of one year plus one day. Location - This role is in-person. Work primarily takes place at North Campus, Edmonton. The Clinical Research Coordinator is responsible for the day-to-day coordination and conduct of clinical trials and investigator-initiated research studies, from participant recruitment through study close-out. Working under the direction of the Principal Investigator, the coordinator recruits, consents and screens study participants, performs study-specific assessments, manages ongoing participant follow-up, and ensures all study activities are conducted in accordance with the approved protocol, International Council on Harmonisation (ICH) Good Clinical Practice (GCP) guidelines, National Institutes of Health (NIH) guidelines, and institutional policies. The coordinator maintains regulatory and study documentation, serves as the primary point of contact for study sponsors and monitors, coordinates with hospital departments including radiology, laboratory, pharmacy, health records and nursing, and maintains detailed time sheets allocating effort across studies. The position requires the ability to manage multiple concurrent protocols independently in a fast-paced clinical environment, and to work effectively with team members as the research program may grow in the future.