4 Manage roles in Oracle Clinical One Platform
- Oracle Clinical One Platform web address
You receive the web address (URL) for signing in to Oracle Clinical One Platform in an email after an administrator assigns the product roles to you in Oracle Life Sciences IAMS. - Sign in and out of Oracle Clinical One Platform
You sign in using your Oracle Life Sciences single sign-on (SSO) user name and password. You receive your Oracle Life Sciences SSO details over email after your SSO is created. - Create study user accounts
To create a study user in Oracle Clinical One Platform, a delegated administrator must create an Oracle Life Sciences single sign-on (SSO) in Oracle Life Sciences IAMS, assign roles, and then add the user to the appropriate study. Whether the user works at the sponsor, CRO, site, or depot, the workflow for creating the user account is the same. - Study roles in Oracle Clinical One Platform
Study roles represent a collection of permissions that, when assigned, let users perform their tasks in the system in an efficient manner, without compromising the study blind. - Edit a study role that is already assigned to users
As a global user manager or study user administrator, you can edit an existing study role created for both all studies or just an individual study, even if the study role is already assigned to users. - Retire a study role
Study roles can never be completely removed, but they can be retired. If a study role is no longer of use in your study, you can always retire it. Users who have previously been assigned the now retired study role will not lose their permissions. Retired study roles are simply made unavailable for new use. - Remove a user in Oracle Clinical One Platform
In Oracle Clinical One Platform, you can remove a study user (someone who is assigned to one or multiple studies) or you can remove a global user (someone who is assigned a global role and may have access to all studies in your organization). - Specify data classifications for a study role
Data classifications allow you to control which users can view or edit a specific type of question in the study. As a global user administrator or study user administrator, you can assign specific permissions to users depending on what type of classified data they should get access to.