Site User

This topic describes the permissions included in the Site User (template) study role in the application. This template study role is available for all studies in your organization. You can copy the study role and customize it for each individual study you work in.

Note:

To see an overview of all permissions that can be included in study roles, see the View Permissions window in the application.

Table 8-12 Site User (template) study role

Category	Permissions assigned
CRF Submit Access	Confirm download of the Archival PDF Download the Archival PDF Run the Archival PDF for your site
Clinical Data Collection	Add a Lab to a Site Add and Update Lab Normal Ranges Answer Queries Approve and sign subject data Create and Add Labs to a Site Dispense Kits with Calculated Doses Dispense Kits without Calculated Doses Edit Classified Subject Data Only Edit Form Data for Subjects Edit Visit Dates Randomize Subjects Skip Visits Take Action on Connected Devices Unblind the Treatment Arm for a Subject, or Code Break View Blinded Dispensation Details with Calculated Doses View Blinded Dispensation Details without Calculated Doses View Classified Subject Data Only View Form Data for Subjects View Queries
Inventory Management	Create Manual Shipments Perform Supplies Reconciliation at Site Receive Shipments and Update Site Inventory View Shipments to Sites View Site Inventory
Notifications	Receive Notification of Shipments Receivce the Code Break Notification Receive the Dispensation Notification Receive the Randomization Notification Receive the Subject Screening Notification Receive the Subject Transferred Notification Receive the Subject Visit Notification Receive the Subject Withdrawal Notification
Reports	Run the Blinded Inventory Report Run the Enrollment Report Run the Kit Dispensation Report Run the Kit Reconciliation Report Run the Order Summary Report Run the Subject Data Report Run the Subject Events Report Run the Subject Query Report Run the Subject Visit Report Run the Titration Summary Report Run the Training Report Run the User Assignment Report
Study Management	Create Shipments to DDF