- 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 entered into database is consistent with the source data.
For interested candidates, please send your updated resume:
