ROUEN
About 8 years of experiences in clinical research (since 2006). Significant clinical study site monitoring experience in both hospital and different Clinical Research Organisation as Study Coordinator, CRA, Sn CRA, and Mentor. Since 2 year, the Lead CRA role has offered me the possibility to provide my monitoring expertise to study team and Monitors to improve the site quality oversight.
Through training, co-monitoring and regular monitor meetings, I help to ensure the quality and integrity of the data collected in the clinical trials to ensure successful monitoring of the trial.
I have worked during 5 years in the Urology TA and since October 2014, I work in the Ophthalmology TA for large international studies (phase III).
Pas de formation renseignée
