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Clinical Research Manager (CRM) Sweden, København Denmark, Vantaa Finland, Norway,  

IRW (company)

Posted on : 10 July 2017

Project Description

desirable qualifications and background

principal duties
  • Planning, coordination and execution of projects 
  • lead the study team and ensure that study deliverables are met 
  • managing project budget 
  • assist the study team during audits and inspections 
  • prepare and complete Applications to the regulatory authorities and ethic committees 
  • prepare and conduct pre-study activities, selection and initiation visits, routine monitoring and close out visits 
  • selecting and negotiating contracts with sites, local/central laboratories, pharmacies etc. 
  • Training of staff 
  • Planning, participating and leading investigators meeting 
  • writing and preparing the clinical study Documentation 


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

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