Sandra Courbier

  • Social Research Director - Rare Barometer Programme Lead

Sandra Courbier

Sandra Courbier joined EURORDIS as Patient Voices Manager in June 2015, later becoming Social Research Director - Rare Barometer Programme Lead. She is based in the Paris office.

She is responsible for consulting patients and their representatives to support advocacy and policy-making activities at EURORDIS. This is mainly done through the Rare Barometer programme which consists of surveys aiming to collect qualitative & quantitative data on the experience and expectations of rare disease patients and their families to facilitate and streamline the inclusion of patient perspectives into EURORDIS advocacy work. She also facilitates the generation of patient opinions on ethical, legal and social issues around rare disease research through European Commission-funded research projects.

Prior to joining EURORDIS, Sandra worked for the French Governmental information service, obtaining a broad experience of health-related surveys and studies, public communication and public affairs. While working for TNS Opinion in Brussels, the company responsible for the Eurobarometer, she also gained knowledge on international survey research.

She holds a master in survey methodology applied to political science and sociology from the Institut d’études politiques de Grenoble. Sandra speaks French and English. 

 

Telephone: +33 1 56 53 52 63
Email: sandra.courbier@eurordis.org

 
 
La voz de los pacientes de enfermedades raras en EuropaEURORDIS La voz internacional de las personas que tienen enfermedades rarasRare Disease International Reuniendo a pacientes, familiares y expertos para compartir experiencias en un foro moderado en distintos idiomas. RareConnect El Programa Rare Barometer es una iniciativa de EURORDIS que realiza encuestas para transformar las experiencias de los pacientes con enfermedades raras en cifras que puedan compartirse con los responsables políticos.Rare Barometer Una campaña internacional de sensibilización que se celebra todos los años el último día de febrero, El Día de las Enfermedades Raras es una iniciativa de EURORDISRare Disease Day Únete al mayor grupo de partes interesadas en toda Europa, en la Conferencia Europea sobre Enfermedades Raras y Medicamentos Huérfanos que se celebra cada dos años. ECRD es una iniciativa de EURORDISEuropean Conference on Rare Diseases