Add Users

Statistician - Unblinded

View the permissions included in the Statistician - Unblinded template study role. This template study role is of Sponsor type and is available for all studies at your organization.

Note:

You should always copy a template role and begin customizing it within the context of your study. For more information, see About template study roles.

Table 6-13 Permissions included in the Statistician - Unblinded template study role

Category	Assigned permissions
Clinical Data Collection	Edit Classified Subject Data Only View Blinded Dispensation Details with Calculated Doses [Site] View Blinded Dispensation Details without Calculated Doses [Site] View Classified Subject Data Only View Form Data for Subjects View Queries [Site]
Data Extract	Run the Subject Data Extract [Unblind]
Notifications	Receive the Code Break Notification Receive the Unblinded Randomization Notification [Unblind]
Reports	Run the Blinded Randomization Report Run the Blinded Subject Events Dataset Run the Enrollment Report Run the Kit Dispensation Report Run the Study Codelist Dataset Run the Study Design Report Run the Study Query Dataset Run the Subject Data Report Run the Subject Dataset Run the Subject Events Report Run the Subject Form Items Dataset Run the Subject Forms Dataset Run the Subject Query Report Run the Subject Randomization Data Extract Report [Unblind] Run the Unblinded Kits Dataset [Unblind] Run the Unblinded Randomization Report [Unblind]
Study Setup	Edit Regions Upload and Generate Inventory Lists [Unblind] Upload and Generate Randomization Lists [Unblind] View Regions View Role Assignments for Study Users View Sites View Study Design View Study Settings
Unblinded Study Management	Manage Randomization Lists [Unblind] Reveal the Treatment Arm for a Subject or Code View [Unblind]

For more information on each of these permissions, see Descriptions of permissions in Oracle Clinical One Platform.

Parent topic: Template study roles