Clinical Study Coordinator Freelance Nr ref.: /JOBS.pl 0.6-1.0 FTE6 month contract initiallyOffice-basedOne of my clients, international CRO is looking for Clinical Study Coordinator Freelance in Munich.Responsibilities:•Under the supervision of the Principal Investigator who delegates specific tasks, the Study Site Coordinator will provide support to the site staff to ensure that the clinical trial is conducted according to the Protocol, Good Clinical Practices, current regulations and study procedures•Ensuring quality, reliability and authenticity of scientific data collected within the time described by the clinical protocol•Ensuring compliance with safety rules governing clinical trials •Participating in all necessary trainings to carry out the delegated tasks at the investigational centers•Ensuring that the site staff conduct the trial in accordance with the Protocol, existing regulations and procedures •Ensuring logistical aspects of the trial, examples: shipments of tubes to central laboratory or shipment of other materials to other vendors.This is a fantastic opportunity to work for one of the top 10 CRO's currently enjoying strong success in a number of therapeutic areas. For the right candidate the organisation are happy to offer a strong and competitive daily rate, with a good chance of long term contract extension based on individual performance. To apply for this position and put yourself under immediate consideration, send your CV to or call (0) Kontakt: Aplikuj teraz Ogłoszenie pochodzi z serwisu Jobs.pl .
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