Clinical Study Coordinator

Description

Position Summary: Supervises and manages the execution of clinical trials within a research unit, coordinating visits and providing essential support. Key Highlights: 1. Manages and supervises clinical trials 2. Coordinates patient visits and supports committees 3. Actively participates in updating procedures **Job Description** ---------------------- Manage and supervise the execution of assigned clinical trials. This role is performed within the research unit. * Coordinate patient visits for the research area according to protocol * Provide information support to the ethics committee * Coordinate with the clinical laboratory and imaging department for paraclinical tests and diagnostic aids for research patients. * Conduct initiation, monitoring, quality, and study closure visits * Complete the CRF within the timeframe established by the study sponsor * Serve as alternate study coordinator when required * Maintain all institutional and protocol-specific forms updated and at their correct version * Review and submit research protocol documentation to the ethics committee * Participate in updating institutional procedures and guidelines * Keep the research unit’s database updated * Consolidate patient information for reporting and follow-up of serious adverse events to the sponsor and the ethics committee * Maintain updated treatment administration schedules * Maintain inventory and control of devices and equipment * Keep data collection current and resolve inconsistencies * Support the management and supervision of accounting for investigational products when required * Access IVRS or IWRS for reporting subject selection, randomization, selection failure, and discontinuation * Perform role-specific and study-specific activities in accordance with institutional guidelines * Take vital signs, electrocardiograms, and other parameters from research patients * Actively participate in institutional committees and primary teams * Coordinate follow-up meetings for research processes * Request creation and/or updating/deletion of process-related forms and documents as part of the quality management system * Train other study coordinators on center and study activities and conduct follow-up. **Candidate Requirements** -------------------------- * Health professional. * 2 years of experience in activities related to academic training * 1 year of experience in clinical research * English level: A2; B1 preferred. * Knowledge of regulatory requirements * Patient assessment and monitoring * Participation in multidisciplinary health teams * Research bioethics * Clinical research methodology * Epidemiology (preferred) **Selection Process** ------------------------ The selection process is conducted through Aira — a recruitment platform designed to enhance your application experience. To apply, you only need: 1. Apply to the position 2. Check your email 3. Log in to Aira and answer the requested questions and/or tests Then, if your profile matches our requirements, we will contact you by email (via Aira) to proceed to the in-person stage. **About Us** ------------------ Auna is a leading organization whose primary commitment is to deliver health and wellbeing to its members and patients. We pursue continuous innovation to provide high-quality, accessible health solutions for everyone. We operate in Peru, Colombia, and Mexico and have over 14,500 employees. At Auna, we work with an integrated, person-centered healthcare model—the most important pillar of our mission. **Our Benefits** ----------------------- * Medical insurance * Training programs and courses * Wellness activities * Meal subsidy * Product discounts