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Administracja biurowa » Pracownik biurowy

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Opis:

Clinical Research Associates CRA II/SCRA - in the Czech Republic Nr ref.: /JOBS.pl The key responsibilities of a Clinical Research Associate (CRA) are to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations, performing clinical on-site monitoring activities, collecting regulatory documentation, performing qualification, initiation, monitoring and termination of investigational sites in accordance with ICH GCP guidelines. Responsibilities & Accountabilities: • Strong computer and internet skills including knowledge of MS-Office products such as Excel & Word. • Strong regulatory knowledge including GCP • Train team members on selected tasks • Take responsibility for specific tasks on projects, or acts as the main CRA contact on individual projects A successful candidate will: • Be educated to a degree level in a life science • Be competent in both written and oral English • Have substantial monitoring experience within the field of clinical research For further information on this position or to have a confidential conversation please contact Simon on (0) or email Key Skills: Clinical Research Associate, CRA, Senior Clinical Research Associate, SCRA, Justpharma, Just Pharma, Monitoring, Clinical Trial, Drug Trial, Trial Sites, Czech Republic, Prague, Monitor, Clinical Research. Kontakt: Aplikuj teraz Ogłoszenie pochodzi z serwisu Jobs.pl .

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