Site Management Associate
Job Summary
Supporting clinical research projects in a hybrid role, the full-time Site Management Associate will streamline communication, manage documents and information, and serve as the main point of contact for site personnel and vendors in Bogot , Colombia.
Key responsibilities
- Act as the primary contact for site personnel and CRA, facilitating query resolution and EDC completion
- Ensure the completion of pre-study testing and manage clinical supplies, including order, receipt, and inventory
- Coordinate regulatory submissions and manage the Trial Master File (TMF) at both site and country levels
Required qualifications
- College/University Degree in Life Sciences
- Administrative work experience, preferably in international settings
- Prior experience as a Clinical Trial Assistant (CTA) for Contract Research Organizations (CROs)
- Knowledge of local regulations related to clinical research
- Full working proficiency in English and proficiency in MS Office applications
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