seguenti figure professionali: ClinicalResearchAssociate I (CRA I); ClinicalResearchAssociate II (CRA II...); Senior ClinicalResearchAssociate I (sCRA I). Per tutte le figure, è previsto un inserimento diretto in azienda, a tempo...
: ClinicalResearchAssociate I (CRA I); ClinicalResearchAssociate II (CRA II); Senior ClinicalResearchAssociate... mesi di esperienza e formazione specifica sul clinical trial); pregressa esperienza (almeno 1-2 anni) e autonomia nel...
seguenti figure professionali: ClinicalResearchAssociate I (CRA I); ClinicalResearchAssociate II (CRA II...); Senior ClinicalResearchAssociate I (sCRA I). Per tutte le figure, è previsto un inserimento diretto in azienda, a tempo...
Are you a dedicated ClinicalResearchAssociate looking to advance your career in a role that values your expertise... months of experience as a ClinicalResearchAssociate. – Fluent in English and Italian to effectively communicate...
As a Senior ClinicalResearchAssociate you are responsible for monitoring clinical trials and ensuring investigators... are conducting research within the requirements of the clinical protocol and ICH-GCP. You will be involved in all stages of clinical...
, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinicalresearch... as they relate to the conduct of clinical trials. Current in-depth knowledge of regulations governing clinicalresearch, ICH/GCP...
, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinicalresearch... as they relate to the conduct of clinical trials. Current in-depth knowledge of regulations governing clinicalresearch, ICH/GCP...
and techniques for clinicalresearch Good English communication Good knowledge of MS Office Suite TECHNICAL COMPETENCES & SOFT... on client clinical projects, producing high quality deliverables to agreed timelines, while following relevant standard...
As a ClinicalResearchAssociate (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...
As a ClinicalResearchAssociate (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...
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