Clinical Trial Coordinator
Current• Coordinate local and multi-centre clinical trials in accordance with Good Clinical Research Practice (GCRP) and International Conference of Harmonisation (ICH) guidelines• Assist with the identification of potentially eligible patients and inform the medical staff of the screening procedures for study entry.• Coordinate patient appointments and clinical follow-up, the collection of data, the collection of specimens and collation of test results and the immediate reporting of serious adverse events.