As a Clinical Research Coordinator, you will provide support for research studies through the identification, collection, and reporting of clinical trial data. You will compile research, reports and regulatory documents as required by the protocol, and study/sponsor. This involves ensuring research information is timely, accurate, valid, meaningful, and to the sponsor’s satisfaction, and that studies are run according to local and global regulations.
Classification: Clinical Resrch Coord (ACB)
Union: HSAA Facility PROF/TECH
Unit and Program: Tom Baker Cancer Centre (TBCC) CRU Indirect Cost
Primary Location: Tom Baker Cancer Centre
Multi-Site: Not Applicable