The Clinical Study Administrator (CSA) assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives
Ensures essential documents under their responsibility are uploaded in a timely manner to maintain
the eTMF “Inspection Readiness”.
and supports the CRA in the close out activities for the ISF.
Assists in coordination and administration of clinical studies from the start-up to execution and close- out.
• Operational responsibility for the correct set-up and maintenance of the local eTMF and ISF including document tracking in accordance with ICH-GCP and local requirements
and ensures successful conduct of responsibilities
and appropriate interactions with internal and or external customers.
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