Anne-Laure Aslanian

  • Patient Engagement Manager Healthcare – ERN & Healthcare / European Patient Advocacy Groups

Anne-Laure Aslanian joined EURORDIS in March 2019 as Patient Engagement Manager. She is managing and supporting 8 out of the 24 European Patient Advocacy Groups (ePAGs) that were set up by EURORDIS to ensure a meaningful patient advocates’ engagement across all European Reference Networks (ERNs) activities.  Anne-Laure also leads the communication and knowledge management activities to support the 24 ePAGs’ work and facilitate exchange of good practices and access to information.

Anne-Laure has several years of experience in research and innovation project management and development of international research project proposals. Prior to joining EURORDIS, she worked for 4 years in a hospital research institute and in a biomedicine center in Barcelona to foster the participation of researchers and clinicians in research grants opportunities and to enhance their collaboration in European healthcare initiatives.

She holds a Master’s degree in European Studies and International Business Law from Aix-Marseille University (France).

She is a native French speaker, she also speaks English, Spanish, Catalan and basic Portuguese.

Telephone: +34 93 220 48 60
Email: anne-laure.aslanian@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