Tasks

  • Assists the clinical operations team in the operational management and oversight of clinical trials, during set-up, conduct and until archiving, for an assigned trial
  • Coordinate site contracts finalization, preparation, and distribution of study documentation/materials
  • Ensure accurate maintenance and archiving of the electronic Master File (eTMF)
  • Support tracking of activities
  • Organize coordinator shipment
  • Finance: support review and tracking of invoices, PO creation, etc
  • Perform other duties as assigned

Qualifications

  • Bachelor or Master Studies in natural science, e. g. biology, chemistry, pharmacy, medicine or similar
  • Interest to dive into Clinical Research
  • Very good organizational skills
  • Attention to detail and quality
  • Fluent in English