Clinical Research Training for Senior CRAs

In this two-day course, you receive an update of the current European legislation on clinical research, you learn how to upgrade monitoring methods and skills, how to select the right investigators, how to boost recruitment of clinical trial subjects, how to solve site management issues and how to deal with non-compliance. You gain insights in monitoring plan development, tracking tools, accurate monitoring visit reporting, safety reporting and how to be prepared for audits and inspections.

This course has been specifically designed for people with at least 2 years’ experience as a Clinical Research Associate (CRA) and who want to set new goals and objectives in their career.