Site Management Associate I
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About the role
Hybrid Site Management Associate I role in Buenos Aires supporting international clinical research projects. Responsibilities include site and vendor coordination, CTMS updates, clinical supply management, regulatory and ethics submissions, audit and inspection preparation, TMF/ISF management, training coordination, document and translation tracking, and safety information flow. A college/university degree in Life Sciences, CTA experience in CROs, clinical research experience, local regulations knowledge, English proficiency, and MS Office proficiency are required.
Key requirements
- • College/University Degree in Life Sciences
- • Required skills: Administrative work experience, Prior experience working as a Clinical Trial Assistant (CTA) for contract research organizations (CROs), Prior experience working in clinical research, Knowledge of local regulations, Full working proficiency in English, Proficiency in Microsoft Office applications, Planning and working in a dynamic team environment, Communication and collaboration skills
- • Required language: English
Opportunity details
- • Workplace: Hybrid
- • Posted: Nov 12, 2026
- • Original advert language: English
Full vacancy
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See original vacancy ↗Employer’s role description
Job title: Site Management Associate I
Location: Buenos Aires, Buenos Aires, Argentina
Employment type: Full-time