Site Management Associate I

This is a fully remote position, open to applicants in Argentina.

📋 Description

• Serve as the primary support for clinical research initiatives

• Enhance communication, uphold systems, and manage documentation and information

• Act as the central liaison between site staff and the Clinical Research Associate (CRA)

• Provide assistance in the preliminary evaluation of local site facilities

• Oversee the ordering, receipt, inventory storage, distribution, return/recall, and reconciliation of clinical supplies

• Ensure compliance with regulatory requirements and ethics committee submissions

• Coordinate preparations for and follow-up on audits and inspections

• Manage the Trial Master File (TMF) at both the site and country levels

⛳️ Requirements

• Bachelor’s degree in Life Sciences

• Experience in administrative roles, ideally in international environments

• Previous experience as a Clinical Trial Assistant (CTA) for Contract Research Organizations (CROs)

• Background in Clinical Research

• Knowledge of local regulations

• Full working proficiency in English

• Competence in MS Office applications

• Ability to plan and collaborate effectively in a dynamic team setting

🏝️ Benefits

• Propel your career forward in the field of clinical research

• Manage a diverse range of tasks

• Acquire new knowledge while advancing with the company