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Tmf Specialist Document Management Specialist Mfd

Miltenyi Biotec - Bergisch Gladbach Germany

Full-time

Not Disclosed

In this role you will be responsible for collecting reviewing maintaining and archiving essential regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP) E6 ICH Guidelines and other regulatory guidance documents and Clinical Trials Regulati More...

Employer Active Posted on 20 Dec | Full-time | Easy Apply

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