info@irwcro.com | +46 8 791 66 40

Desirable qualifications and background

  • Academic degree in natural science such as medicine, pharmacist biomedicine 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