Data Manager

View the permissions included in the Data Manager 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.

A user who is assigned this template study role template can also manage tasks related to integrations between Oracle Clinical One Platform and:

A third-party electronic data capture system
Oracle Life Sciences InForm
Veeva Vault CTMS
Oracle Siebel Clinical Trial Management System

Table 6-5 Permissions included in the Data Manager template study role

Category	Permissions assigned
CRF Submit Access	Run and Download Site Confirmation and Download Log Audit Reports Run and Download all PDF Request Types and Audit Reports. Enable Share with Sites, and Site Confirmation
Clinical Data Collection	Add a Lab to a Site [Site] Add and Update Lab Normal Ranges Create and Add Labs to a Site Edit Classified Subject Data Only View Classified Subject Data Only View Form Data for Subjects View Queries [Site] Note: When a data manager is assigned the Edit Classified Subject Data Only permission, they have the ability to edit forms that don't contain classified data. Advise data managers to only work with the forms that contain classified data.
Data Extract	Run the Subject Data Extract [Unblind]
Notifications	Receive the Code Break Notification Receive the Pending Signatures Notification Receive the Study Limits Notifications Receive the Subject Completion Notification Receive the Subject Number Update Notification Receive the Subject Rollover Notification Receive the Subject Undo Completion Notification Receive the Subject Undo Screen Failure Notification Receive the Subject Undo Withdrawal Notification
Reports	Run the Blinded Chain of Custody Report Run the Blinded Randomization Report Run the Blinded Subject Events Dataset Run the Kit Dispensation Report Run the Lab Normal Range 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 Events Report Run the Subject Form Items Dataset Run the Subject Forms Dataset Run the Subject Query Report Schedule Reports to Run
Settings	Manage Signature Settings
Study Management	Close All Queries Close Auto Queries (planned for a future release) Close Queries By Role (planned for a future release) Create Candidate Queries Create Queries Delete Candidate Queries Freeze subject data entered at a site Lock subject data entered at a site Unfreeze subject data entered at a site View All Queries
Study Setup	View Role Assignments for Study Users View Study Design View Subject Settings

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

Parent topic: Template study roles