Production Admin

View the permissions included in the Production Admin 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 6-9 Permissions included in the Production Admin template study role

Category	Assigned permissions
Clinical Data Collection	Add a Lab to a Site [Site] Add and Update Lab Normal Ranges Create and Add Labs to a Site Integrate Subject Data View Blinded Dispensation Details with Calculated Doses [Site] View Blinded Dispensation Details without Calculated Doses [Site] View Form Data for Subjects View Queries [Site]
Inventory Management	Create Shipments to Depots [Unblind] Create and Manage Dispensation Exceptions Receive New Shipments at the Depot Release Shipments from Quaratine Update the Shipment Order Form View Shipments to Sites View Site Inventory
Reports	Run the Blinded Chain of Custody Report Run the Blinded Inventory Report 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 Site and Depot Report Run the Study Codelist Dataset Run the Study Design Report Run the Study Query Dataset 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 Training Report Run the Unblinded Chain of Custody Report [Unblind] Run the Unblinded Inventory Report [Unblind] Run the User Assignment Report Run the User Upload Error Report Schedule Reports to Run
Rules Management	Re-run Rules
Settings	Configure Connected Device Study Settings Edit Welcome Details in General Study Settings Manage Signature Settings
Study Setup	Assign a Resupply Strategy to a Depot Assign a Resupply Strategy to a Site Assign a Study Version to a Site Create and Manage Lots [Unblind] Create and Manage Sites Edit General Study Settings Edit Regions Edit Study Settings Edit Supply Settings, Blinded Groups, Label Groups, and Resupply Strategies [Unblind] Manage Archives Settings Move a Study Design to Testing or Production Upload and Generate Inventory Lists [Unblind] Upload and Generate Randomization Lists [Unblind] 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]
Unblinded Study Management	Manage Randomization Lists [Unblind] Update Inventory Lists [Unblind]

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

Parent topic: Template study roles