Description:
The main purpose of the post is to conduct monitoring visits at participating trial sites to ensure that: the rights, safety and well-being of human subjects are being protected, reported trial data are accurate, and the trial is being conducted in compliance with the protocol and applicable regulatory requirements, including Good Clinical Practice. The postholder will work on specific CTC trials with on-site/remote monitoring requirements and will also support CTC trial teams in the preparation of monitoring documentation and assist with centralised monitoring of documents submitted by trial sites.