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Adding Clinical Trial Subjects and Managing Subject Visits and Activities

Sites can enter information about clinical trial subjects. After the subject record is added, the subject visit template active for the site can be applied to set up a schedule of visits and activities for the subject.

Sites users perform the following tasks to add clinical trial subjects and manage their visits and activities:

  • Add subjects to protocols.
  • Screen and rescreen subjects to generate subject visits and activities.
  • Enroll subjects.
  • Mark subject activities completed.
  • View subject calendars.
  • Monitor subject status and enrollment rates.
Siebel Life Sciences Portals Guide