Job Description
職務說明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. 資歷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 and spoken). Good interpersonal skills, a good team player, and computer skills. Be able to prioritize and manage multiple tasks.
Date Posted
26-Feb-2026Closing Date
29-Jun-2026