Medical Monitor

View the permissions included in the Medical Monitor 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 6-6 Permissions included in the Medical Monitor template study role

Category	Permissions assigned
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]
Notifications	Receive the Code Break Notification
Reports	Run the Blinded Subject Events Dataset 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 Events Report Run the Subject Form Items Dataset Run the Subject Forms Dataset Run the Subject Query Report Run the Training Report Run the User Assignment Report
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 View All Queries
Study Setup	View Role Assignments for Study Users View Sites View Study Design View Study Settings
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