Experience

Covance Central Laboratory Services SA
• Switzerland
• Biotechnology Research
• 1 - 100 Employee
• Senior Global Study Manager

  • Jun 2019 - Present


Covance CLS

• Project Manager

  • Aug 2008 - Present

  • Act as the primary liaison between Sponsor and Covance and manage consequently the Covance assigned study team (Project Coordinator, Technical Administrator…). • Accountable for the review of the clinical protocol to define feasibility, assess risk and provide consultative approach for the database design. • Responsible for the study set-up and database design and closely monitor critical study milestones. • Pro-actively manage the assigned budget and take appropriate actions. • Manage day-to-day project related activities.



Hopitaux du Leman

• France
• Medical Practices

• Clinical Research Associate

  • Jan 2008 - Jul 2008

  • Key contact for INCA (Institut National du Cancer) to set up Clinical Trial Department • Participating to Physician meeting • Identify patient to be recruited • Provide Physician training • Ensures that all physicians are compliant with protocol requirement • Follow up of patients including in clinical trial set up • Ensures that eCRF/CRF are correctly completed and documentation is up to date • Key contact for INCA (Institut National du Cancer) to set up Clinical Trial Department • Participating to Physician meeting • Identify patient to be recruited • Provide Physician training • Ensures that all physicians are compliant with protocol requirement • Follow up of patients including in clinical trial set up • Ensures that eCRF/CRF are correctly completed and documentation is up to date



Schering-Plough Research Institute

• United States
• Pharmaceutical Manufacturing
• 400 - 500 Employee

• Clinical Research Associate

  • Jun 2006 - Dec 2007

  • Management of phase II, III and long term follow-up clinical trials in hepatology, and infectious diseases indication, from initiation study visits to close out visits: • Responsible of EC and HA submission • Coordinate study budget and set up contracts with hospital and physicians, investigators payments • Monitoring of study treatment • Write study related documents: Inform consent, summary of protocol. • Training on GCP/ICH guidelines • Manage day-to-day project related activities