Site Activation Partner I - FSP

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Site Activation Partner I - FSP based in Brazil. This role offers an opportunity to support clinical research studies from site start-up through study close-out, ensuring activities are completed accurately, efficiently, and in compliance with applicable requirements. You’ll work closely with investigator sites, study teams, regulatory stakeholders, and other partners to facilitate successful site activation and ongoing study operations. A key focus will be managing essential documentation, regulatory submissions, ethics processes, and site readiness activities within required timelines. You’ll also help maintain high-quality trial records and support sites throughout the study lifecycle. The position combines independent ownership with close collaboration across international clinical research teams. It is particularly suited to professionals with strong site activation experience and knowledge of US/Canada clinical trial requirements.