2015 - 2015Clinical trials- (Phase III) in Oncology & Neurology & Ophthalmology
- Site Monitoring visits
- Monitoring visits of pharmacy: checking the delivery of therapeutic units, products and materials, Quality-check of the pharmacy file
- Site Initiation Visits
- Writing reports of visits
Coordination of International Clinical trials (Phase III) in Ophthalmology and Cardiology
- Feasibility studies
- Assist in the Submission process to Ethic commitees
- Site Selection visits
- Site Initiation Visits
- Writing reports of visits
- Assisting in Preparation & Negotiation of contracts: Contracts Management; contact with centers for clarification of the study protocol, negotiation of additional costs and investigators fees, finalization of contracts
- Budgets Tracking,
- Management of the logistics initiation visit and opening of centers: establishment of Greenlights for sending therapeutic units
- Preparing Study documents(CDA, FDF, FDA Form 1572)
- Close out visits
Coordination of International Clinical trials (Phase IV) in Neurology
- Assist in the submission to CCTIRS, CNIL
- Preparing study documents (ICF)
Centre Régional de Pharmacovigilance de Franche-Comté
- Ingénieur Qualité- Stagiaire
2014 - 2014Développement du système qualité du centre régional de Franche-Comté :
Rédaction du cahier des charges
Audit clinique
Analyse de l’évolution des déclarations des effets indésirables liés aux médicaments
Actualisation des procédures de recueil des déclarations des effets indésirables liés aux médicaments
Amélioration de la traçabilité des déclarations des effets indésirables liés aux médicaments
Construction d’un indicateur qualité