Elisabeth Garrison has extensive work experience in regulatory affairs and life sciences. Elisabeth has been working at Blueprint Medicines since 2018, initially as a Senior Manager in Regulatory Affairs and currently as an Associate Director in Global Regulatory Sciences (GRS) Strategy. Prior to that, they worked at Voisin Consulting Life Sciences (VCLS) as a Senior Regulatory Scientist and later as an Associate Director in Clinical Regulatory. Elisabeth also gained experience at ANSM Agence nationale de sécurité du médicament et des produits de santé as a Regulatory Assessment trainee, at Servier as a Medical Writing trainee, at Hôpital Necker-Enfants Malades as a Pharmacy intern, and at Sanofi-aventis as a Regulatory Affairs trainee.
Elisabeth Garrison completed their education at Paris-Sud University (Paris XI) from 2005 to 2011, earning a Pharm.D. degree in the field of Pharmaceutical Industry. In addition, they obtained certification in ICH-GCP from the Royal College of Physicians in January 2015.
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