Clinical Research Coordinators


Shanghai, Nanjing, Chengdu, Changsha, Tianjin, Changqun


The CRC often handles the bulk of the daily study activities and plays a key role in the study conduct and management. The CRC is frequently responsible for organizing the documentation and files pertaining to a study and for coordinating the activities of the investigators and the study participants.

The responsibilities of the CRC may include:

  • To initiate, monitor and close-out clinical trials in accordance with all relevant GCP standards and regulations;
  • To record and archive properly all clinical trial related activities;
  • To complete and review Case Report Forms (CRF) and ensure their validity, accuracy and integrity;
  • To assist in the management of clinical trial product and related documents.


  • Bachelors degree or higher in medical, pharmaceutical, nursing or related field, preferably with 1 year working experience in hospital;
  • Knowledge of medical terminology and clinical patient management;
  • Good oral and written skills in English;
  • Excellent computer knowledge of Windows operation system, MS Office software and Internet applications;
  • Good interpersonal and organizational skills;
  • Ability to work both independently and work within a team;
  • Knowledge of ICH-GCP, and/or CRA experience is a plus.
Apply for this position >>