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Clinical Research Associate (CRA) - Sweden, Denmark, Finland, Norway  

IRW (company)


Posted on : 10 July 2017

Project Description

Desirable qualifications and background
  • Academic degree in natural science such as life sciences 
  • Experience from pharmaceutical, biotechnology or medical device industries 
  • Experience from Clinical Research Organizations (CRO) 
  • Good ability to express yourself both verbally and in writing 
  • Good knowledge of spoken and written English 
  • Good organizational skills 
  • A service-minded approach 
  • Ability to prioritize and handle several tasks simultaneously 
  • Valid driving license 

Principal duties
  • Prepare and complete applications to the regulatory authorities and ethic committees 
  • Prepare and conduct pre-study activities, site selection and initiation visits, routine monitoring and close out visits 
  • Negotiate contracts with sites, local/central laboratories, pharmacies etc. 
  • Manage assigned sites throughout the study to ensure site compliance, adequate enrolment, and understanding of study requirements 
  • Participate in Audits and Inspections 
  • Assist in data validation and clean file procedures 
  • Planning and participating at Investigators meeting 
  • Responsible for final archiving of study documents in-house and on-site