Clinical Research Coordinator, NUHCS (CTU)

Overview To assist investigators in conducting clinical trials and research according to study protocol, ICH Good Clinical Practice (ICH GCP), Singapore Human Biomedical Research Act (HBRA) and other applicable regulatory and ethical requirements as well as hospital policies. Roles and Responsibilities Primary Responsibilities and Duties (90%) 1. Compliance with the ICH GCP, HBRA and other applicable regulatory and ethical requirements as well as hospital policies if applicable. 2. Patient Mana…

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