Study Monitor

6 days ago


Fatih, Istanbul, Turkey PDC CRO Full time
Main Responsibilities
  • Participate in feasibility studies with delegated tasks from FS responsible;
  • Site selection and qualification evaluation under supervision of senior personnel;
  • Assist during study set-up regarding submission and approval process and preparation of documentation as per local requirements;
  • Collect all ECs requirements per allocated studies;
  • Coordinate, assist (if needed), and participate in any trainings and meetings related to specific studies;
  • Monitor and quality control of investigational sites; planning and performing monitoring visits in accordance with GCP and study protocol;
  • Review and reporting of non-compliances/protocol deviations, AE/SAEs to sponsor, and taking responsibility for accurate performance of SDV process;
  • Reporting of trial progress to CPM by writing reports and collecting trial-specific data;


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