Experience

FAST4

• France
• Research Services
• 1 - 100 Employee

• Chef de Projets

  • Oct 2016 - Present

• Digital Clinical Research Associate

  • Feb 2015 - Oct 2016



Sanofi

• France
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Trial Operation manager

  • May 2014 - Dec 2014

  Clinical trial coordinator - management of IP Clinical trial coordinator - management of IP



Orfagen subsidiary of Pierre Fabre

• Région de Toulouse, France

• Clinical Research Associate

  • Oct 2012 - Sep 2013

  Site initiation visit on a phase III study. (France, Germany, Italia, Sweden, Austria). Monitoring visits independently: Control and collection of CRF papers and data sources, update of Investigator's file and Pharmacist's file. Control and collection of the investigational products. Site coordination. Management of queries. Writing of Monitoring guidelines and CRF completion guidelines. Submission of a study amendment to the Ethics Committees and the Competent Authorities. Investigator's training. Preparation and participation of a blind review. Show less



Galderma

• Clinical Trial Administrator

  • Apr 2012 - Sep 2012

  Implementation and follow-up of Trial Master Files. Submissions of a phase I clinical trial to the Ethics Committee. Site initiation visit. Review and Quality Control of protocols and subject documents Implementation and follow-up of Trial Master Files. Submissions of a phase I clinical trial to the Ethics Committee. Site initiation visit. Review and Quality Control of protocols and subject documents



C.H.U Arnaud de Villeneuve

• Région de Montpellier, France

• Clinical Research Associate

  • Jan 2012 - Feb 2012

  Screening, Inclusion and follow-up of subjects. Filling of CRF and eCRF Audit Screening, Inclusion and follow-up of subjects. Filling of CRF and eCRF Audit