Clinical Research Associate

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.