Position Overview
Primarily responsible for coordinating the various aspects of clinical trials. Works as part of a clinical delivery team providing support, guidance and advice on a local level. Develops existing tools and processes to identify areas of improvement and ensures business continuity for study delivery. Able to solve complex problems within a range of studies.
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Be responsible for initiating, organizing and managing the assigned studies.On site monitoring and site managements for global studies.Ensure clinical trials conducted in compliance with protocol & GCP.Ensure clinical trials can be conducted per timeline requirement.θ³ζ·
Bachelor degree or above, major in pharmacy or health science related background.At least 2 year experience in the role of CRA including on-site monitoring.With knowledge in GCP clinical therapeutics, study methodology, GCP.Excellent command of English (both written ...