Responsibilities

• To ensure compliance with the Singapore guidelines for Good Clinical Practice, Human Biomedical
• Research Act and all relevant MOHs Act & Guidelines.
• Possess a sound and in-depth understanding of the protocol of the assigned registry
• To prepare Domain Specific Review Board (DSRB) applications and make ongoing amendments to the registry.
• To review the inclusion/exclusion criteria with the custodian of the registry.
• To explain objectives of data collection to participant and obtain informed consent.
• To closely monitor participants outcome, track their follow-up visits and ensure data collected for post-op is within acceptable period.
• To prepare data for doctors research study.
• To ensure assessment for each participant is accurate and complete.
• To ensure data ent...