サイトモニター / SSU

Job Details

Job Summary

Responsible for the oversight of the progress of a clinical trial.

Responsibilities

・Oversite of the clinical trials.
・Conducting, recording and reporting with the protocols and SOPs, GCP.

Qualifications

・Demonstrates a thorough understanding and knowledge of all steps in the clinical research process.
・Knowledge of GCP, ICH as well as local regulations.
・Site Monitor / SSU – 2-3 years industry related experience as site monitor