Josee Hue-Perron

Associate Principal Scientist at Debiopharm
  • Claim this Profile
Contact Information
us****@****om
(386) 825-5501
Location
Lausanne, Vaud, Switzerland, CH
Languages
  • English Full professional proficiency
  • French Native or bilingual proficiency

Topline Score

Topline score feature will be out soon.

Bio

Generated by
Topline AI

You need to have a working account to view this content.
You need to have a working account to view this content.

Credentials

  • European Registered Toxicologist
    EUROTOX
    Apr, 2020
    - Nov, 2024
  • DABT
    American Board of Toxicology, Inc.
    Nov, 2022
    - Nov, 2024

Experience

    • Switzerland
    • Pharmaceutical Manufacturing
    • 300 - 400 Employee
    • Associate Principal Scientist
      • Jan 2022 - Present

      Nonclinical toxicologist in drug development, from early in vitro assays to preclinical studies supporting up to commercialisation. Coordinate and lead CRO relationship. Nonclinical toxicologist in drug development, from early in vitro assays to preclinical studies supporting up to commercialisation. Coordinate and lead CRO relationship.

    • Belgium
    • Biotechnology Research
    • 700 & Above Employee
    • Preclinical Safety Lead
      • Oct 2018 - Dec 2021

      Nonclinical toxicologist in drug development, from early in vitro assays to preclinical studies supporting up to Phase III. Coordinate and lead CRO relationships Nonclinical toxicologist in drug development, from early in vitro assays to preclinical studies supporting up to Phase III. Coordinate and lead CRO relationships

    • France
    • Research Services
    • 100 - 200 Employee
    • Head of Toxicology In vivo
      • May 2014 - Oct 2018

      Management of In vivo Tox operations, a team of 70 technicians, team leaders and trainers. Act as the scientific liaison between technicians and scientists Development and validation of new techniques and procedures in a GLP environment.

    • Senior Study Director
      • Jan 2013 - Oct 2018

      Study Director for all types of preclinical studies. Elaborate study plans and reports according to the regulations and Sponsor’s needs. Collaborate with the technical groups to improve techniques and procedures.

    • Study Director
      • Mar 2012 - Jan 2013

      Study Director

    • United States
    • Biotechnology Research
    • 700 & Above Employee
    • Study Director
      • Apr 2006 - Mar 2012

      Study Director

    • Assistant Scientist
      • Jan 2005 - Apr 2006

      Study Director on short term non-GLP studies Draft study protocols and reports. Collaborate with the technical groups to improve techniques and procedures.

    • Technician
      • May 2001 - Jan 2005

      Technician in infusion, pharmacology and neurotoxicology Performing surgeries, dosing via different routes

Education

  • Université de Montréal
    DESS, Toxicology
    2007 - 2010
  • Université du Québec à Trois-Rivières
    BSc, Medical Biology
    2002 - 2006
  • Cégep de la Pocatière - CEC de Montmagny
    Technicienne, Santé Animale
    1998 - 2001
  • École Secondaire Mont Saint-Sacrement
    Diplôme d'études secondaires
    1993 - 1998

Community

You need to have a working account to view this content. Click here to join now