
The Quality Issue Lead role within Parexel FSP focuses on managing quality events and investigations across the US and Canada. The position involves triaging submitted cases to determine if they meet quality thresholds, conducting thorough root cause and gap analyses, and ensuring timely documentation within the eQMS system. Key responsibilities include escalating critical issues to senior management, developing CAPA plans to track mitigation effectiveness, and contributing to process improvements and training materials. This position appeals to professionals seeking a remote work arrangement with opportunities to drive continuous improvement in clinical trial quality. The role requires a strong background in pharmaceutical GCP and GxP regulations, offering a chance to lead investigations and enhance operational efficiency within a collaborative team environment.




















