Opis stanowiska
As a Clinical Research Associate (CRA) you are an essential part of the clinical operations team responsible for coordinating and overseeing the execution of studies and clinical trial according to the study protocol, ICH-GCP, applicable regulations, guidelines and sponsor requirements. Some of what you will do: Identify investigator sites and participate in the feasibility process for new studies Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accorda…
Szczegóły oferty
Data publikacji
14.06.2025
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