About this role
Job title: Assistente de Operações Jr. ( Cronogramas )
About the Role The selected candidate will be responsible for supporting the planning and conduct of clinical studies, ensuring methodological compliance and operational excellence. They will work on the elaboration and management of clinical study timelines, trainings and follow-ups, organizing and launching internal agendas to ensure planning effectiveness and timely delivery of results within established deadlines. They will also assist with the registration of studies in the Scheduling System, updating study reservation calendars and controlling dates for data submission, statistical reports and final sponsor reports. Additionally, they will actively contribute to reducing rework in the area’s routines, ensuring traceability, compliance and integrity of records in alignment with Good Clinical Practice (GCP).