Includes but is not limited to: Coordination and supervision of clinical studies, ensuring compliance with protocols and good clinical practices. Consolidation of performance indicators (recruitment, deviations, safety) and preparation of corporate reports. Review and verification of inclusion and exclusion criteria to optimize identification and selection of eligible patients. Implementation and monitoring of corporate recruitment plans to accelerate participant enrollment. Review and maintenance of up-to-date source documents to ensure accuracy and traceability. Support in monitoring activities, including preparation and organization of documentation, accompaniment during monitoring visits, and follow-up of corrective actions arising from findings. Coordination and support for site qualification visits (SQV) and site initiation visits (SIV), ensuring site readiness, availability of essential documentation, and compliance with sponsor requirements. Position type: Full-time Experience: * Clinical studies coordination: 1 year (Desirable) Language: * English (Mandatory) Location: * Barranquilla, Atlántico (Mandatory) Willingness to travel: * 100% (Desirable)