Paloma Tejada

  • Rare Diseases International Director

Paloma TEJADA

Paloma Tejada joined EURORDIS in 2007 as Communications Manager later becoming Communications Director. After one year of parental leave, Paloma rejoined EURORDIS on a part time basis as Rare Diseases International Senior Manager.

Paloma is part of the Governance team, working on the launch and development of Rare Disease International.

Paloma has extensive experience working for not-for-profit and non-governmental organisations in Europe, America and Asia. Previously she worked for Medecins du Monde as a Programme Manager for their international HIV/AIDS network.

She was also a Programme Coordinator for Appropriate Technology Asia in New Delhi where she managed a water and sanitation programme in Tibetan refugee settlements.

After obtaining a Bachelor of Arts in Communications from the American University in Washington DC, she went on to complete a Master of Science in Development Management at the London School of Economics.

A dual Peruvian-French national, she grew up in Lima and has lived in Paris since 2002.

She is fluent in English, French and Spanish.

Telephone: +41 763 60 47 25
Email: paloma.tejada@eurordis.org

 
 
La voix des patients atteints de maladies rares en EuropeEURORDIS Donnant la voix, à l'international, aux personnes vivant avec une maladie rareRare Disease International Pour rapprocher patients, familles et experts sur un forum modéré multilingue, où partager leurs expériences. RareConnect Le programme Rare Barometer est une initiative d’EURORDIS qui vise à réaliser des sondages pour transformer les expériences des patients de maladie rare en faits et chiffres à communiquer aux décideurs politiques.Rare Barometer Campagne internationale de sensibilisation organisée chaque année le dernier jour de février, la Journée Internationale des Maladies Rares est une initiative d'EURORDISRare Disease Day Participez au plus grand événement réunissant tous les acteurs des maladies rares en Europe lors de Conférence européenne bisannuelle sur les maladies rares et les médicaments orphelins (European Conference on Rare Diseases and Orphan Products, ou ECRD). L'ECRD est une initiative d'EURORDISEuropean Conference on Rare Diseases