Anne 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.

  • Clinical experience gained in one of the biggest CRO, leading a clinical data team
  • 6 years’ experience managing partnership projects for a French network of scientists and clinicians in the field of lymphoma
  • PhD in Life Sciences from the University of Geneva, Switzerland while working at the biotech company Merck Serono on preclinical projects in autoimmune and inflammatory diseases