Medical Monitor

View the permissions included in the Medical Monitor template study role. This template study role 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 predefined study roles.

Table 8-6 Permissions included in the Medical Monitor template study role

Category Permissions assigned

Clinical Data Collection

  • Edit Classified Subject Data Only
  • Safety Case Submit (planned for a future release)
  • View Blinded Dispensation Details with Calculated Doses
  • View Blinded Dispensation Details without Calculated Doses
  • View Classified Subject Data Only
  • View Form Data for Subjects
  • View Queries

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
  • Close Queries By Role
  • 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