Klinischer Forschungsmitarbeiter/Klinischer Forschungskoordinator
Responsibilities The CRA/CRC is responsible for the monitoring or auditing of all activities subject to the, „ICH Good Clinical Practice: Konsolidierte Richtlinie,“ (GCPs), supporting client programs administrated by Watermark ensure project data and summary statements are of known and documented quality. Requirements Will be expected to travel extensively to study Weiterlesen

