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Clinical Research Manager (CRM) - Sweden, Denmark, Finland, Norway  

IRW (company)


Posted on : 10 July 2017

Project Description

Desirable qualifications and background
  • Academic degree in natural science such as medicine, pharmacist bio medicine or similar 
  • Experience from pharmaceutical, biotechnology or medical device industries 
  • Experience from Clinical Research Organizations (CRO) 
  • A well developed understanding for customer care and business development 
  • 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 

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