모집분야

담당업무

자격 요건

Central Monitor

1. During study planning and start up

ž   Support the study project management team by contributing to the identification of protocol critical data and processes

ž   Preparation and review of the study central monitoring plan

2. During study conduct:

ž   Conduct periodic reviews of aggregate clinical trial data, as described in the central monitoring plan, to include, but not limited to, data listings, key risk indicators.

ž   Provide direction to site monitors for additional remote and on-site monitoring activities for risk sites, within the scope of the trial monitoring and central monitoring plans

ž   Conduct periodic review, as described in the central monitoring plan, of aggregate data for trends within a site to further support RCA CRA and direct monitoring activities

ž   Must have worked as a clinical research practitioner for a minimum of 2yrs in an operational function e.g. data management, clinical monitoring, medical monitoring

ž   Must have a proven track record of successful delivery, including effective management and understanding of data, and accountability for quality and timelines.