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A question about Data Manager Role
From: "Michel Acosta"
To: [email protected]
Date: Mon, 02 Dec 2013 20:38:09 +0000
Subject: A question about Data Manager Role
I have a question about the Data Manager Role. In The Clinical Trial Process only the sponsor can choose the staff, in OpenClinica it can be done by Data Managers and by the Study Director. What can I do to avoid data managers to add users to system and to studies, keeping the ability of creating CRFs (they do carry out this task in the process).
If anybody think that the current way is correct, please explain me why. I´ll appreciate it. I´m responsible for providing a software for managing information obout clinical trials in my working center, I think OpenClinica is very very good but this point could be a disadvantage in case of a regulatory entity audit.
Thanks in advance.
Ing. Michel Acosta.