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You will coordinate clinical trial activities according to the study protocol and in line with ICH Good Clinical Practice guidelines and local health regulations. You will support the Principal Investigator with patient screening and recruitment, monitoring subject compliance with treatment and follow-up, and collecting and managing data including resolving discrepancies. You will also coordinate the collection of biological specimens, monitor adverse events and safety reporting, and maintain investigator site files. Additional duties include preparing submissions to the ethics committee and health authorities, and tracking trial expenditures and invoicing.
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