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CRA Spain - Italy  

OPIS (company)

Posted on : 06 April 2017

Project Description

Location Barcelona, Spain Job Description We are looking for an experienced CRA with expertise in performing on-site pre-study, initiation, monitoring and close-out visits according to ICH/GCP, regulatory and protocol specific requirements. Qualifications Bachelor or higher degree in life sciences, nursing or medical technology At least 2 years monitoring experience of clinical studies Phase I  IV/observational studies ICH/GCP knowledge, basic understanding of regulatory affairs Full understanding of Serious Adverse Event (SAE) reporting and follow-up of SAEs Good planning, organization and problem solving abilities Good communicative and interpersonal skills Willingness for travel including overnight stays where necessary Fluent in Spanish and English


Desio (MB) Italy

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