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Clinical Trial Administrator

Full-Time Vietnam, Vietnam
Health & Biotech
Health & Biotech
27 March 2025
Description
Support the clinical team's inhouse activities on assigned projects. Organize and manage study-related documentation to ensure proper record-keeping. This includes tracking files, preparing for internal and external reviews, conducting quality checks, and ensuring all records are properly stored according to standard guideline. Support with collecting, translating, and managing important study documents following standard guidelines and procedures Maintain and update the project management system, ensuring all records related to research sites, study progress, and participant tracking are accurate and up to date. Prepare and distribute study materials (e.g., patient instruction cards and diaries, lab supplies, drug supplies, etc.) and track their usage to ensure smooth operation
Qualifications
Relevant experience/qualifications in Life Sciences or related field or administration would be preferable. Work experience at a Korean company is preferred. Experience working in the pharmaceutical, CRO((Contract Research Organization), healthcare industry, and Korean company is advantageous. Must be proficient in speaking, writing and reading Korean. Beginner-level English proficiency, including basic reading and writing, is acceptable.
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