Research Manager AplusA Real World
PharmD with Master in clinical studies (Université Claude Bernard, Lyon).
Since 2017 she supports the AplusA Real World Department with her pharmaceutical and regulatory background as Research Manager.
In this position, she is responsible for reviewing material, checking the local regulatory framework and assisting in the submission to local EC/IRB. She also brings her added value for study management and adverse event reporting.
Her legal expertise is very valuable for regulatory processes for NIS.