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Julie BAYLE

PARIS 13

En résumé

R&D projects management
- Proof-of-concept (in vitro/ in vivo)
- Preclinical and clinical development of therapeutic products (human drugs) or nutritional solutions (feed)
- Project Management :
* Study director (POC, preclinical, human clinical phase)
* Outsourcing management (CRO and public or private scientific collaborations)
* Planning, managing resources to achieve specific goals, budget, SWOT, risks analysis
* Quality : SOP writing, BPL and BPC studies
* Project Documentation, patent follow-up…
* Funding: national or international projects (ANR, ISI…), et de (OSEO, CIR…)
* Organizes and leads internal and external meetings
* Publications writing (10)

Specialties: Immunology, Cancerology, Genetics, Metabolism
Toxicology
Signaling Tyrosine Kinase Receptor
Drug delivery system
Nutritional support

Mes compétences :
Clinical Development
DIRECTOR
Drug Delivery
Immunology
Products
Oncologie
Nutrition animale

Entreprises

  • INSERM - PhD

    PARIS 13 maintenant

  • Royal Canin - Scientific communication manager, region of emergents contries

    AIMARGUES 2018 - maintenant

  • Royal Canin - Research Project manager

    AIMARGUES 2012 - maintenant Health nutrition for animals (MARS Petcare)
    R&D-Discover team: program leading to new nutritional solutions, diagnostic tools, scientific knowledge (dogs and cats with pathologies/ veterinary pilar)
    - Literature review (scientific expertise, patents, symposia, articles...)
    - Design of study protocols (research contract, ethics review committee, logistic...)
    - Study report (database, statistical analysis...)
    - International collaboration with KOLs (private and public lab)
    - Internal & external communication (presentation to internal customer, congress, publications...)
    - Member of Ethics Review Committee

  • MEDESIS PHARMA - R&D Project Manager

    2007 - 2012 Project management, coordination of preclinical and clinical studies on antidiabetic products (Biotech Company/ startup).
    o Preclinical duties: Proof of concept, efficacy studies on animal models, PK studies, toxicological studies (writing of protocol/reports); ethical committee
    o Clinical duties (phase I-II):  Set-­up & follow-­up of clinical trial;  synopsis & IB writing; documents reviewing (IMPD/ CRF...);  sponsor TMF gestion; data review, central lab selection...
    o Finances : contract/NDA/MTA management, budget follow-up,
    o Outsourcing activities (selection & relation with CRO and collaborators)  
    o Bibliography follow-­up ; SOPs writing (quality system)
    o GLP/GMP/GCP compliance

  • Boston University School of Medicine - Postdoctoral Fellow

    2005 - 2007 Duties: Molecular mechanisms of skin fibrosis in Scleroderma patients and Tsk mouse model; investigating especially on the SFRP4 and potential role of Wnt signaling in skin fibrosis

    Conduct of in vivo & in vitro experimental studies, writing papers & grants…

Formations

Pas de formation renseignée

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