Director, Global Clinical and Pharmacovigilance Quality Assurance @ (January 2015 - January 2020)
Clinical Project Manager @ (January 2010 - January 2014)
Clinical Research Associate @ (January 2009 - January 2010)
Clinical Research Associate @ (February 2008 - September 2009)
Initiative and Feasibility Associate @ Pfizer (July 2007 - January 2008)
Naïma Said Education
Institut national agronomique Paris-Grignon
Sup Santé
Naïma Said Skills
Affaires réglementaires
Audit qualité
Biotechnologie
Bonnes pratiques cliniques
CIH - BPC
CRO
Clinical Development
Clinical Monitoring
Clinical Research
Continuous Improvement
Corrective and Preventive Action (CAPA)
Cross-functional team leadership
Documents règlementaires
Driving Results
Développement clinique
Essais cliniques
Informatisation des essais cliniques
Pharmacovigilance
Quality system
Recherche clinique
Regulatory Requirements
SOP
Sciences de la vie
Secteur pharmaceutique
Surveillance clinique
Team Management
Validation
Informatisation Des
Cih Bpc
Cih
Bonnes Pratiques
Bpc
Naïma Said Summary
Naïma Said, based in Paris, FR, is currently a Senior Director Quality Assurance at Ividata Life Sciences. Naïma Said brings experience from previous roles at Roche, LYSARC, DBV Technologies and Novo Nordisk. Naïma Said holds a Institut national agronomique Paris-Grignon. With a robust skill set that includes Affaires réglementaires, Audit qualité, Biotechnologie, Bonnes pratiques cliniques, CIH - BPC and more.
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