sCRA at a bio pharmaceutical company
Spring Professional
15 일 전


  • Monitoring of investigational sites and the Clinical Monitoring Plan for each study
  • Assist Project Manager with identification, site feasibilities, and selection of investigational sites
  • Preparing site essential documents, and participates in the ethics and regulatory submission and approval processes
  • Train investigators on the sponsor and regulatory requirements for conducting the study
  • Ensure any error or omission in study procedure at site is appropriately documented
  • Ensure project tracking systems are updated to reflect work performed at clinical trial site
  • Provide general clinical support to the clinical project teams
  • Main Requirements

  • Bachelor’s degree or higher
  • 3-10 years of working experience in related field
  • Experienced and worked as a clinical research associate previously
  • Good communication skills
  • Native in Korean
  • Please kindly send your CV to Shokhrukh Jobborov at j.shokh or call 010-6729-7757 for a private discussion.


    Consultant : Shokhrukh Jobborov

    M : 010-6729-7757

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