**About the position:** **Working hours:** Monday to Thursday from 8:00 AM to 6:00 PM and Friday from 8:00 AM to 5:00 PM **Work model:** CLT - 100% in-person **Main Responsibilities:** * Perform submission of amendments and notifications (document review, signature collection, document upload on Plataforma Brasil) * Complete and update the master spreadsheet; * Prepare semi-annual reports and submit them to PB; * Verify CEP approval/rejection (release of opinion), file the document in the study binder and on the network; * Respond to document pending issues via Plataforma Brasil; * Complete CRFs and resolve queries; * Receive monitors, provide forms, and accompany monitoring visits together with the coordinator; * Resolve monitoring letters; * Assist with screening scheduling; * Perform medication releases (when necessary) through IWRS; * Schedule biological sample collections and assist in their processing if applicable; * Assist the clinical research analyst in coordination-related activities, such as: scheduling patient visits in the Vita Primo system, preparing visit scheduling spreadsheets, registering the study in Vita Primo, and verifying procedures in the system; monitor study safety reports; transmit imaging exams to the appropriate platforms for each study; * Conduct relevant sector and clinical study trainings; * Participate in department meetings Job type: Permanent CLT Pay: R$2,500.00 - R$2,800.00 per month Benefits: * Medical insurance * Dental insurance * Private pension plan * Life insurance * Meal allowance * Transportation allowance Selection question(s): * What is your level of English? Education: * Pursuing or incomplete higher education (Mandatory) Experience: * Clinical Research (Mandatory)