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Responsibilities:

Communicate and collaborate on global study activities working closely with the project coordinator and clinical trial manager
Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
Compile and maintain project-specific status reports within the clinical trial management system
Interact with the internal project team, Sponsor, study sites, and third-party vendors
Provide oversight and quality control of our internal regulator

Associate Clinical Trial Manager - PhD / Post-Doc (Oncology)