Overview

The Clinical Research Associate is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close‑out. The role involves building a relationship with the site, being the sole position accountable for site performance, driving the site successfully to initiation, developing a robust patient recruitment strategy, setting up a system, assessing compliance with regulations and the site’s capability to meet study needs and recruitment expectations, and problem‑solving to address and resolve site issues.

This may include various tasks and roles within the CRA framework, contingent upon project phase and country demands, and complexity of the study. The Clinical Research Associate will oversee the conduct of the trial at designated sites, ensuring the rights and well‑being of human subjects are protected, evaluating the quality and integrity of the reported data, evaluating site staff t...