La Faculty Completa




Elenora Ingrassia

Clinical Study Manager presso Chiesi Farmaceutici
Management of clinical research across Europe (phase III, observational studies) principally in respiratory and musculoskeletal area.

The activities include:

  • Writing protocols and clinical report;
  • Developing full documents from the study outline and coordinating the CRO activities.
  • Manuscripts revision and congress presentations of abstracts and posters.
  • Cooperation with QA, legal department and other relevant functions.
  • Provide with professional support to the planning and organization of investigator meeting, data reviews and any other study-relevant meeting.
  • Drug supply management
  • Study budget: contributing to budget planning with the relevant persons in charge of budget by providing cost estimation, forecast & budget
  • revision and reconciliation.
  • Contributing to the selection of CRO and/or Providers

 

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