Experience

Urosphere
• France
• Biotechnology Research
• 1 - 100 Employee
• Chief Operating Officer

  • Jun 2022 - Present


Pierre Fabre Group

• France
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Head of Non Clinical Strategy

  • Jan 2019 - Jul 2022

  - Identification of the Non-Clinical Strategy for the Established and Consumer Health Care products (innovation and valorisation).- Scientific evaluation of new assets for inclusion in the development pipeline.- Identification of partners, setting up and management of collaborations. - Management of the dedicated budget- Scientific communications in international conferences

• Head of Scientific Outsourcing

  • Apr 2016 - Jan 2019

  - Identification and Implementation of the Pierre Fabre scientific outsourcing strategy.- Management of 15 Outsourcing Managers.- Identification of preferred partners and setting up collaborations. - Pharmacological expertise for all the Pierre Fabre Group areas (Dossier Evaluation, Experimental design, Project analysis….).

• Pharmacology Laboratory manager / Study Director

  • Jan 2011 - Apr 2016

  - Planning and management of innovating preclinical projects - Pharmacological characterization and development of drug candidates.- Research and selection of CROs, monitoring of outsourced studies. - Team management / Carrier management. - Scientific communications in international congress and publications.- Analysis and interpretation of the results.- Collaborations with internationals key opinion leaders.- Framework in transverse mode (GLP environment).

• Pharmacological Scientist

  • 2008 - 2011

  - Development and carrying out preclinical in vivo and in vitro studies.- Audit and statistical analysis of the results.- Redaction of study reports.- Interaction with internal and external sponsors and contractors.- Regulatory environment



UROSPHERE

• France
• Biotechnology Research
• 1 - 100 Employee

• Pharmacological Scientist

  • Jan 2006 - May 2008

  - Development and carrying out preclinical in vivo and in vitro studies. - Audit and statistical analysis of the results. - Redaction of study reports. - Interaction with internal and external sponsors and contractors. - Regulatory environment. - Development and carrying out preclinical in vivo and in vitro studies. - Audit and statistical analysis of the results. - Redaction of study reports. - Interaction with internal and external sponsors and contractors. - Regulatory environment.



Organon

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Pharmacological Scientist

  • Jan 2005 - Dec 2005

  - Development and carrying out preclinical in vivo and in vitro studies. - Audit and statistical analysis of the results. - Redaction of study reports. - Interaction with internal and external sponsors and contractors. - Regulatory environment. - Development and carrying out preclinical in vivo and in vitro studies. - Audit and statistical analysis of the results. - Redaction of study reports. - Interaction with internal and external sponsors and contractors. - Regulatory environment.