Sandra Courbier

  • Rare Barometer survey programme Senior Manager

Sandra Courbier

Sandra Courbier joined EURORDIS as Rare Barometer survey programme Senior Manager in June 2015 and 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

 
 
The voice of rare disease patients in EuropeEURORDIS The international voice of people living with rare diseasesRare Disease International Bringing together patients, families and experts to share experiences in a moderated multi-language forum. RareConnect The Rare Barometer Programme is a EURORDIS initiative that carries out surveys to transform rare disease patients' experiences into figures and facts that can be shared with decision-makers.Rare Barometer An international awareness raising campaign taking place on the last day of February each year, Rare Disease Day is a EURORDIS initiativeRare Disease Day Join the largest gathering of rare disease stakeholders across Europe, at the biennial European Conference on Rare Diseases and Orphan Products. ECRD is a EURORDIS initiativeEuropean Conference on Rare Diseases