View Only for Unblinded Support Users

This topic describes the permissions included in the View Only for Unblinded Support Users (template) study role in the application. This template study role is available for all studies in your organization. You can copy the study role and customize it for each individual study you work in.

Typically assigned to a member of the Health Sciences Support who should assist with troubleshooting, this study role can also be found as a predefined template, at a global level. Alternatively, you can also create your own study role that might be different from the predefined one, at either a global level or in the context of a study.

Note:

To see an overview of all permissions that can be included in study roles, see the View Permissions window in the application.

Permissions given to a Health Sciences Support user

Table 8-17 View Only for Unblinded Support Users (template) study role

Category Permissions assigned

Administrative

  • View Only for Unblinded Support Users
Clinical Data Collection:
  • Edit Classified Subject Data Only
  • 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

Data Extract

  • Run the Subject Data Extract

Inventory Management

  • View Shipments to Sites
  • View Site Inventory
  • View Unblinded Pharmacist Kits

Reports

  • Run the Blinded Inventory Report
  • Run the Blinded Subject Events Dataset
  • Run the Data Collection Design Dataset
  • Run the Enrollment Report
  • Run the Kit Dispensation Report
  • Run the Kit Reconciliation Report
  • Run the Kits and Randomization Design Dataset
  • Run the Order Summary Report
  • Run the Site and Depot Report
  • Run the Study Codelist Dataset (planned for a future release)
  • Run the Study Design Report
  • Run the Study Query Dataset
  • Run the Study Rules Report
  • Run the Subject 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
  • Run the Subject Visit Report
  • Run the Training Report
  • Run the Titration Summary Report
  • Run the Unblinded Chain of Custody Report
  • Run the Unblinded Inventory Report
  • Run the Unblinded Kits Dataset
  • Run the Unblinded Subject Events Dataset
  • Run the Unblinded Subject Visit Schedule Report
  • Run the Unblinded Titration Summary Report
  • Run the User Assignment Report
  • Schedule Reports to Run
Rules Management
  • Re-run Rules

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

Unblinded Study Management

  • Reveal the Treatment Arm for a Subject, or Code View