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Desirable qualifications and background

  • Academic diploma/degree in natural science such as life sciences, pharmacy or nursing.
  • Previous experience of working in the Pharmaceutical/CRO industry
  • Awareness of GCP/ICH Guidelines and other applicable regulatory requirements.
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
  • Good ability to express yourself both verbally and in writing
  • Good knowledge of spoken and written English and local language
  • Good organizational skills
  • A service-minded approach
  • Ability to prioritize and handle several tasks simultaneously
  • Valid driving license
  • Position might require occasional travel

Principal duties

  • Assist Project managers and Clinical teams with accurately updating and maintaining clinical systems.
  • Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation, folders and reports
  • Assist clinical teams with the development of site tools and clinical trial start up activities.
  • Assist Clinical teams in preparation, handling and distribution of Clinical Trial Supplies
  • Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
  • Performs other related duties and tasks, as required.