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Siebel Clinical Trial Management System Guide > Setting Up a Clinical Trial > Scenario for Clinical TrialsThis scenario is an example process performed by the director of clinical trials, clinical study manager, and the clinical research associates (CRAs). Your company might follow a different process according to its business requirements. In this scenario, the clinical director and the study manager, working for a clinical research organization, or pharmaceutical, biotech, or medical device company, have administrator responsibilities in Siebel Clinical to:
NOTE: The tasks of entering subject data, and setting up screening and enrollment visit schedules for subjects, can also be performed by the site personnel using Site Portal Web site. For more information about Siebel Site Portal, see Siebel Life Sciences Portals Guide. At various times after subjects have been enrolled in the trial, the clinical director, study manager, or CRAs can use the charting features of Siebel Clinical to review the progress of the trial. Two informative metrics are the subject status and enrollment rate. These are plotted for an individual site, for a region, and for the protocol. |
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