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Clinical Study Assistant

Oxford Global Resources - Utrecht
handle, distribute, file, and archive clinical documents and reports according to GCP guidelines and standard operating procedures.Prepare Study Files Get ISF (investigator site file) and TMF (trial master file) ready for the
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Clinical Research Coordinator

IQVIA - Utrecht
is expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies
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Clinical Research Coordinator

IQVIA - Tiel
expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the
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