View Only for Unblinded Support Users

View the permissions included in the View Only for Unblinded Support Users 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.

Typically assigned to a member of the Life Sciences Support team who should assist with troubleshooting, this study role can also be found as a predefined template at a global level. Support users who are assigned the View Only for Unblinded Support Users (template) template study role are automatically updated with any new permission introduced for a given release.

Table 6-18 Permissions included in the View Only for Unblinded Support Users template study role

Category	Assigned permissions
Administrative	Run the Study Roles Report View Only for Unblinded Support Users [Unblind]
CRF Submit Access	Download Archival PDFs, and Audit Reports [Site] Run the Archival PDF for your site(s) [Site]
Clinical Data Collection	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	Execute ODM Administrative Data API Execute ODM Clinical Data API with Hidden Data [Unblind] Execute ODM Clinical Data API without Hidden Data Execute ODM Metadata API Run the Subject Data Extract [Unblind]
Inventory Management	View Dispensation Exceptions View Shipments to Sites View Site Inventory View Unblinded Pharmacist Kits [Unblind]
Reports	Run the Blinded Chain of Custody Report Run the Blinded Inventory Report Run the Blinded Kits Dataset Run the Blinded Randomization Report Run the Blinded Subject Events Dataset Run the Enrollment Report Run the Kit Dispensation Report Run the Kit Reconciliation Report Run the Lab Normal Range Report Run the Order Summary Report Run the Site and Depot Report Run the Study Codelist Dataset Run the Study Design Report Run the Study Query Dataset Run the Study Rules Report Run the Subject Data Report Run the Subject Data for CTMS 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 Subject Visit Report Run the Supply Prediction Report [Unblind] Run the Titration Summary Report Run the Training Report Run the Unblinded Chain of Custody Report [Unblind] Run the Unblinded Inventory Report [Unblind] Run the Unblinded Kits Dataset [Unblind] Run the Unblinded Randomization Report [Unblind] Run the Unblinded Subject Events Dataset [Unblind] Run the Unblinded Subject Visit Schedule Report [Unblind] Run the Unblinded Titration Summary Report [Unblind] Run the User Assignment Report Run the User Upload Error Report Schedule Reports to Run
Rules Management	Test Custom Rules
Study Management	View All Queries
Study Setup	View Depots View Regions View Role Assignments for Study Users View Sites View Study Design View Study Settings View Supply Settings, Blinded Groups, Label Groups, and Resupply Strategies [Unblind]
Trial Management	Note: All permissions listed in this category are planned for a future release. View Actions on Trial Management Event Records View Blinded Trial Management Records View Trial Management Event Records View Unblinded Trial Management Records [Unblind]
Unblinded Study Management	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