FSP CTM Brazil

The FSP CTM Brazil will manage all clinical operational and quality aspects of allocated studies, ensuring compliance with ICH GCP. Responsibilities include developing clinical tools, contributing to the Master Action Plan, and ensuring the quality and timely setup of the Trial Master File. The role involves collaborating with project managers and clinical teams, implementing standardized monitoring processes, and managing clinical activity timelines and metrics to achieve final deliverables within contractual periods. The position also requires continuous monitoring of clinical trials, potential site coordination, managing start-up activities, and ensuring crucial document quality meets regulatory expectations. Additionally, the FSP CTM Brazil will be responsible for clinical resource management and assignment.