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CRA Spain - Italy  

Company managed [?] Still accepting applications
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Posted on : 06 April 2017

Project Description

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. 

  • 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