Coordenador de Centro de Pesquisa Clínica

Coordinate daily execution of clinical studies, ensuring visit schedules, procedures, and recruitment targets are met. Monitor active study statuses to identify risks and implement action plans while distributing operational tasks and tracking progress. Support research coordinators, nurses, pharmacists, and study assistants; facilitate continuous team training and recruitment strategy monitoring. Guarantee compliance with ICH-GCP, current regulations, and standard operating procedures. Prepare the center for monitoring visits, audits, and regulatory inspections; maintain up-to-date study documentation and respond to sponsor and auditor requests. Participate in study tracking meetings.