WuXi AppTec

  • Clinical Research Associate I

    Job Locations CN-Shanghai
    Job ID
  • Overview

    The Clinical Research Associate I (CRA I) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.


    • Implements and monitors local clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH‐GCP guidelines
    • Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and close clinical trials at investigative sites
    • Reviews and verifies accuracy of clinical trial data collected, either onsite or remotely
    • Provides regular site status information to team members, trial management, and updates trial management tool.
    • Completes monitoring activity documents as required by Company or Sponsor SOPs or other contractual obligations
    • Works closely with other clinical team members to facilitate timely resolution of trial and/or clinical issues
    • Escalates site and trial related issues per Company SOPs, until identified issues are resolved or closed
    • Performs essential document site file reconciliation
    • Performs source document verification and query resolution
    • Assesses IP accountability, dispensation, and compliance at the investigative sites
    • Verifies Serious Adverse Event (SAE) reporting according to trial specifications and relevant local and ICH GCP guidelines
    • Communicates with investigative sites
    • Updates applicable tracking systems
    • Ensures all required training is completed and documented
    • Be assigned logistical support tasks by CTM for Investigator Meetings



    Requirements for position

    • A Master's degree in a health care or other scientific discipline or educational equivalent
    • Industry experience preferred.
    • IDE-PMA and/or IDE-510k monitoring experience strongly preferred.
    • Research certification and/or program completion desired
    • Alternatively, you should have an equivalent combination of education, training and experience
    • Read, write and speak fluent English and Mandarin.


    Equal Opportunity Employer Minorities/Women/Veterans/Disabled


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