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Site Management Associate I

πŸ•’ 9 days ago
Clinical ResearchCommunicationDocumentation ManagementRegulatory Compliance

πŸ“œ Description

  • Streamline communication between site personnel and CRA for query resolution and EDC completion.
  • Serve as the primary contact for vendors, study supplies, and access management.
  • Ensure completion of pre-study testing for local site facilities.
  • Assist Monitors with subject and site event information in CTMS.
  • Manage clinical supplies including order, receipt, inventory, and distribution.
  • Coordinate regulatory submissions and ensure compliance with local regulations.

πŸ› οΈ Requirements

  • College/University Degree in Life Sciences;
  • Administrative work experience, preferably in an international settings;
  • Prior experience working in Clinical Research;
  • Local regulations knowledge;
  • Full working proficiency in English;
  • Proficiency in MS Office applications;
  • Ability to plan and work in a dynamic team environment;
  • Communication and collaboration skills.
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