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Delete autoexecution task

The autoexecution tasks added to CTMS to trigger for a certain event—monitoring visit creation or KRI email notification—can be deleted from the system if they are no longer relevant to your study.

Important

You can only delete an inactive autoexecution task.

To delete an autoexecution task

  1. Access the study management page in one of the following ways:

    • In the CTMS application header, select the DASHBOARD tab and then select the study dashboard of your interest.

      Accessing study management from dashboard
      Figure 1. Accessing study management from dashboard

    • In the CTMS application header, select the STUDY MANAGEMENT tab. Then from the Study Data List table, select the study name of your interest.

      Accessing study management from study data list
      Figure 2. Accessing study management from study data list

  2. From the left pane of the study page that opens, select RBM > Auto-execution Engine.

    Accessing autoexecution engine
    Figure 3. Accessing autoexecution engine

  3. In the Auto-execution Task List table that appears, next to the needed autoexecution task, select More more_icon.png > Delete trash_can_icon.png.

    Deleting autoexecution task
    Figure 4. Deleting autoexecution task

  4. In the Reason dialog that appears, provide the details to justify your action. Then select save_button.png.

    Providing reason for task deletion
    Figure 5. Providing reason for task deletion

Once confirmed, the autoexecution task is deleted.

In this section:

An activity in which a monitor, usually a clinical research associate (CRA), visits sites to review and verify study-related activities, including data collection, patient safety, and adherence to the study protocol. The monitor also verifies that the study complies with relevant regulatory requirements and GCP guidelines.

A specific measurement used to monitor and assess potential risks associated with the conduct of the trial. They provide early warning signs of potential issues or deviations that may impact participant safety, data integrity, or the overall success of the study.

Examples of KRIs can be AE report timeliness or query resolution time. The delays in both activities may be considered a sign of the study personnel's neglect. Thus, monitoring is required to ensure the proper conduction of trial activities.