I was trained as a CRA at "For Drug Consulting" school. This training was based on an alternation of theory and simulations of CRA´s missions. I worked at CIC Henri Mondor as a TEC / ARC double rôle. My missions were based in : patients screening and monitoring, CRF and eCRF fill in and checking and tracking data quality, document ranking. I'm now working at Hôpital de Garches as a ARC with missions as initiation visit, monitoring, CRF and eCRF checking and tracking data quality, SAE circuit, queries and reports, document ranking, all in compliance of GCP and reglementations. In addition, I have a strong background in scientific and multidisciplinary research.
Mes compétences :
Biologie moléculaire
Biologie cellulaire
Microbiologie
Biochimie
Immunologie
Microsoft office
Management de projet
Clinical research
Recherche et Développement
Recherche scientifique
Clinical Research Associate
Monitoring