Samira is in charge of clinical study management. Her role is to redact protocols, to prepare studies dossiers for competent authorities and ethical committees within an agreed time, to create supporting documents as informed consents, investigators brochures, and to ensure that studies operations run efficiently with appropriate ISO standards and country/local regulatory requirements.

  • Over 9 years experience in clinical trials coordination in diverse areas
  • Worked in the thoracic oncologic team at the University Hospital of Strasbourg where she was the study coordinator for phase 1 to 4 clinical trials promoted by pharmaceutical companies
  • Samira holds a PhD in Cellular and Molecular Biology; a masters in Biochemistry and a Master in Cellular and Molecular Biology from University Hospital of Strasbourg