Site Management Associate
Job Summary
Serving as the primary contact for clinical research projects, the full-time Site Management Associate will streamline communication, manage documents, and ensure compliance with local regulations while working remotely from Bogota, Colombia.
Key responsibilities
- Act as the main point of contact between site personnel and clinical research associates (CRAs), assisting with query resolution and electronic data capture (EDC) completion
- Coordinate the order, receipt, and inventory management of clinical supplies, ensuring proper distribution and reconciliation
- Manage regulatory submissions and maintain 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 working as a Clinical Trial Assistant (CTA) for Contract Research Organizations (CROs)
- Knowledge of local regulations related to clinical research
- Full working proficiency in English
Complete Job Description
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