Sr. Clinical Research Associate (Australia)

Added
20 days ago
Type
Full time
Salary
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gcp training regulatory filings site monitoring sop
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๐Ÿ“‹ Description

  • Manage and perform full clinical site monitoring for one or more projects.
  • Oversee training, site/patient recruitment, data/document management, and regulatory filings.
  • Act as Lead CRA; liaison between CRAs and project team.
  • Represent the company and maintain stakeholder relationships.

๐ŸŽฏ Requirements

  • Minimum of a college diploma/degree and 4-6 years' related experience.
  • Strong self-motivation with excellent communication skills.
  • Attention to detail and ability to build collaborative relationships.
  • Ability to engage in continuous learning and self-development.
  • Ability to foster teamwork.
  • Dutch language skills for Flemish site support.
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