Site Management Associate I

About the role

Hybrid Bogotá role supporting clinical research projects through site communication, CTMS and document management, clinical supplies coordination, regulatory and ethics submissions, audit and inspection preparation, training tracking, translations review, and safety information flow. Requires a college or university degree in Life Sciences, clinical research experience including prior CTA experience for CROs, local regulations knowledge, and full working proficiency in English.

Key requirements

• • College/University Degree in Life Sciences
• • Required skills: clinical research, site management, regulatory and ethics committee submissions and notifications, local regulations knowledge, English communication, MS Office applications, planning in a dynamic team environment, communication and collaboration, clinical supplies management, document management, clinical trial management systems (CTMS), investigator site file (ISF) management, trial master file (TMF) management, Administrative work experience, Prior experience working as a CTA for CROs, Prior experience working in clinical research
• • Required language: English

Opportunity details

• • Workplace: Hybrid
• • Posted: Sep 23, 2026
• • Original advert language: English

Full vacancy

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