Experience

• 

  Research center of royalieu - technology university of compiègne (utc)

  Oct 1991 - Nov 1995

  Research worker-student (laboratory of enzymatic technology)

  - Brief summary: I imparted translocation properties to model proteins (Enzymes) while keeping their biological activities (Great interest in creating of new medication vectors).

• 

  Kendle international sarl

  Feb 1997 - Nov 2011

  - Participation in proposal preparation (including pricing) and bid defense activities (Attended Bid Defense Meetings in France, UK and US).- Coordination of organization and implementation of clinical projects.- Management of activities between Kendle Operational/Business Units, vendors and clients.- Primary client contact at the project operational level on assigned clinical studies.- Preparation, chairing and follow-up of internal (Kendle) project meetings and external project meeting with vendors and clients.- Project Manager of the European portion of a Phase 2b in Crohn’s Disease (Gastroenterology), a program of 3 European phases 2 and 3 studies in Phenylketonuria (Metabolism/Nutrition), a national Phase 4 study in Musculoskeletal Show less

  • Associate Director, Lab Alliance Management (Project Management Office)

    Apr 2011 - Nov 2011

  • Assignment Manager for EMEA & Asia-Pacific (Global Resource Management – PMO)

    Mar 2007 - Nov 2011

  • Project Leader (Global Clinical Development, Europe)

    Jan 2004 - Feb 2007

  • Manager, Clinical Monitoring (Clinical Operations)

    Dec 2001 - Dec 2003

  • Clinical Research Associate / Lead CRA (Clinical Operations)

    Feb 1997 - Nov 2001
• 

  Covance

  Jan 2012 - Dec 2018

  Senior manager, resource planning (business operations)

  - Responsible for improving and driving mid/long-term resourcing forecasting capacity and management strategy for “Europe-Middle East-Africa”.- Preparation, chairing and follow-up of frequent Resource Management meetings with the Operational Directors and Managers in order to regularly assess business needs and validate recruiting strategies.

• 

  Iqvia france

  May 2019 - now

  - As Acting Resource Responsible Manager (RM), works with the European Clinical Monitoring (CM) Management team to streamline and optimize all resource management related processes, systems and tools as well as to ensure that resourcing data related to the deployment and utilization of staff is as robust as possible to allow an ongoing assessment of workload (demand) in order to determine future resource needs (supply). Participates in the development of recruitment strategies.- As a member of the EU CM Management team, also contributes to broader operational discussions and decisions.- Provides guidance on resource management related processes, systems and tools to other regions. Show less

  • Director, Clinical Monitoring

    May 2021 - now

  • Associate Director, Clinical Monitoring

    May 2019 - Apr 2021