Site Management Associate I
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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
- • Required language: English
Opportunity details
- • Workplace: Hybrid
- • Posted: Sep 23, 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: Bogotá, Bogota, Colombia
Employment type: Full-time
Company Description
We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,800 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.