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Publicat 30 Mai 2007 | Reactualizat 28 Iun 2007 | Expiră 30 Iun 2007

CLINICAL RESEARCH CO-ORDINATOR

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Expirat
-	Co-ordinates studies at country level ; 
-	Maintains the network of clinical research centers ( evaluates, selects and maintains relationships ) ;
-	Handles study feasibilities discussing with investigators, collects submission documents and  analyses what are the potential recruitment considerations;
-	Offers support to centers in study preparation, prepares the recruitment strategies;
-	Participate to investigator’s trainings , coaches the site administrators and facilitates the communication between the site team and the sponsor/ CRO; 
-	Performs direct site management activities: filling in the CRF’s, handling other study documents, ensuring that other members of site team perform their roles properly; 
-	Ensures that centers adhere to all legal requirements, GCP and Synevo operation standards, also that all study procedures are performed in agreement with the study protocol;
               Experience in managing clinical studies performed to GCP;
              Excellent communication / presentation skills; 
              Graduate of the Faculty of Medicine or related academic studies;
              Very good command of English, including medical terminology ;
              Excellent computer skills;
              Driver’s license and willingness to travel.
 CLINICAL RESEARCH CO-ORDINATOR
Expirat
CLINICAL RESEARCH CO-ORDINATOR  -  SC Medicover Rombel SRL

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