Clinical Study Administrator - HCM
On-site · Ho Chi Minh City, Ho Chi Minh City (HCMC), Vietnam
Job Summary
Clinical Study Administrator coordinates and administers study activities from start-up to execution and close-out within the Local Study Team; supports application/documents submissions to EC/IRB and regulatory authorities; manages eTMF/ISF and document tracking; prepares/handles clinical-regulatory documents, CTMS and other systems (e.g., ANGEL, IMPACT, SharePoint); supports study material and equipment coordination; prepares meeting materials and communications; ensures regulatory compliance and timely archiving; works with cross-functional teams and external vendors; requires high school-level qualification and administrative experience in medical/life science fields; English proficiency required.
Required Qualifications
- High school/Secondary school qualifications
- Previous administrative experience preferably in the medical/ life science field
- Proven organizational and administrative skills
- Computer proficiency
- Good knowledge of spoken and written English
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