About the Opportunity:
The Clinical Trial Administrator(CTA) or Inhouse Clinical Research Associate (IHCRA) provides in- house support to the clinical team according to project requirements, ICH GCP guidelines, local or global regulatory requirements and Novotech or Client SOPs.
Responsibilities:
- 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.
Minimum Qualifications & Experience:
- 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.
QUYỀN LỢI
- 18 Annual Leave Days
THÔNG TIN LIÊN HỆ
- Vui lòng liên hệ trực tiếp: Jonghee.Park@novotech-cro.com / +82 2 2143 8732
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