The Clinical Trial Site Operations Working Group aims to establish centralized site supports (for e.g., monitoring, regulatory and ethics support) to enable clinical site research personnel to focus on tasks and responsibilities pertaining to patients.

These support measures will facilitate ACCESS’ aim of providing centralized services to clinical sites to facilitate the local administration and conduct of clinical trials. Moreover, these measures will enhance the recruitment, efficiency, safety and quality of clinical trials at the site-level, thereby making Canadian pediatric cancer centres more enticing sites for the conduct of future investigator-initiated, consortia and industry pediatric cancer clinical trials.