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.