This course explores the key elements of effective collaboration between clinical trial coordinators and monitors.

Focusing on the practical aspects of monitoring visits from the perspective of the clinical trial site, participants will gain insights into optimizing communication, preparing for visits, and addressing common challenges.

It is intended for clinical trial site staff—particularly clinical trial coordinators, study nurses, and investigators—who work closely with monitors (CRAs) and wish to improve the efficiency and quality of their interactions during monitoring visits. The course is also valuable for new monitors seeking a better understanding of the site’s perspective.