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Clinical Research Associate (CRA) Sweden, København Denmark, Vantaa Finland, Norway,  

IRW (company)

Posted on : 10 July 2017

Project Description

desirable qualifications and background

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 


182 17 Danderyd Sweden1310 København K DenmarkRajatorpantie 41 01640 Vantaa FinlandNO 1366 Lysaker Norway

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