Support operational activities related to the conduct of clinical studies, ensuring execution in accordance with protocols, Good Clinical Practice (GCP), applicable national regulations, and current ethical standards. Collaborate directly with the Clinical Study Coordinator and the Principal Investigator to ensure data quality, regulatory compliance, and participant welfare. Support the Clinical Study Coordinator in executing and monitoring protocol-related activities, ensuring ethical and regulatory compliance; Organize, update, and archive essential study documentation, such as logs, forms, and reports; Assist in screening participants according to the inclusion and exclusion criteria defined in the protocol; Record data in Case Report Forms (CRFs) (paper or electronic), ensuring data quality and integrity; Support the management of Investigational Medicinal Products (IMPs); Assist in preparing the site for monitoring visits, audits, and regulatory inspections; Collaborate in reporting adverse events, serious adverse events, protocol deviations, and other regulatory communications; Maintain active communication with monitors, sponsors, and internal teams to provide operational support for studies; Actively participate in developing and updating the department’s Standard Operating Procedures (SOPs); Participate in mandatory training and apply Good Clinical Practice (GCP) principles daily. **Schedule:** 6 days on / 1 day off — Working hours from 09:00 to 17:00. **Minimum Education Requirement:** Bachelor’s degree