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Arnaud BEURDELEY

FONTENAY-SOUS-BOIS

En résumé

- Formation HEC Challenge +
- DESS Management pour Ingénieurs (IIM Paris)
- Dipôme d'ingénieur en Génétique Oncologique (EPHE Paris)
- Maîtrise de Physiologie Animale (Rouen)
- Maitrîse de Biologie Cellulaire (Rouen)

Avril 2006 : Création
Mai 2005-Mars 2006 : Réflexion et maturation du projet "Xentech"
Mars 2003- Octobre 2004 : Responsable Département "Biotechnologies et Industrie Pharmaceutique" - Cabinet Alinéa (Issy les Mlx).
Novembre 2001 - Septembre 2002 : Ingénieur responsable d'un plateforme de PCR quantitative - Molecular Engines Laboratories (Paris).
Janvier 2001 - Octobre 2001 : Ingénieur d'études - Laboratoire d'Oncologie Médicale Hopital Pitié Salpétrière (Paris).
Mars 1998 - Janvier 2001 : Stage d'école d'ingénieur - Institut Curie (Paris).

Mes compétences :
Biologie Moléculaire
Oncologie
Informatique
Création d'entreprise
Biotechnologie
Gestion de projet
Expérimentation Animale

Entreprises

  • Endodiag - Directeur scientifique

    2016 - maintenant
  • InnaVirVax - Chef de projets

    Évry 2014 - 2016 En charge de la logistique de l'étude clinique de Phase II et des études de R&D associées.
  • XenTech - Chef de Projet

    2005 - 2013 www.xentech.fr

    XenTech® is a spin-off of the Institut Curie, the largest French cancer research institute, where its platform has been developed and scientifically validated during the last 10 years.
    With one of the world’s largest collection of clinically relevant human tumor xenograft models, XenTech® reliably evaluates drug candidates, filling the gap between current preclinical models and clinical studies.

    More predictive preclinical models facilitate therapeutic innovation in oncology

    Ethically and economically, reducing late attrition is of major importance in the oncology therapeutic area.
    The success of oncology compounds beyond Phase 1 development largely relies on the molecular relevance of animal models used for preclinical pharmacology studies.
    Panels of tumor models with clinically relevant characteristics defined by genomics and proteomics optimize the chances of success in clinical trials by :

    - excluding ineffective drug candidates early on
    - correctly identifying responsive cancer types
    - identifying synergistic, additive or antagonistic therapeutic combinations
    - allowing biomarker discovery studies for patient stratification in subsequent clinical trials.

    XenTech® experimental platform is based on large panels of well-characterized human tumors directly xenografted onto nude rodents, allowing clinically relevant preclinical studies.

    Preclinical platform
    Our staff has conducted preclinical oncology studies for over 10 years.
    We offer our expertise for the development of your leads:

    - customized approach with a dedicated project manager
    - consulting for protocol establishment
    - high-content molecular database for target expression screening,tumor selection and proof-of-concept studies
    - in vivo and in vitro assays
    - tolerance and efficacy studies
    - biomarker discovery programs

    Facilities
    XenTech® is located in the south of Paris, at Genopole, France’s largest biocluster.
    In vivo studies are conducted at the Center for Exploration and Experimental Functional research (CERFE), a recent SOPF animal facility meeting the latest ethical and technical standards.
    Ethical
    Studies are based on strict scientific and ethical criteria. Confidentiality is guaranteed

    In vivo assays
    Species
    Mice come from certified suppliers with Specific and Opportunistic Pathogen Free (SOPF) status.
    Treatments
    All experiments are performed by experienced technicians under the direct supervision of a dedicated project manager.
    Animal care and housing follow current ethical guidelines.
    Single or combination treatments, with reference chemotherapeutic agents or customer test drugs are routinely performed.
    Follow-up and services
    Animals are followed-up on a daily basis (body weight, general health) with specific measurements adapted to protocols.
    Sampling:
    If included in the protocol, XenTech® can take unique or repeated samples of biological fluids (blood, serum, plasma) or organs for biological assays.
    Results and reporting
    Detailed reports contain all commonly accepted endpoints, contract-determined endpoints and high quality graphics. Each report includes all experimental raw datas, easily interpretable tables and figures, and can be delivered under electronic or hard copy format. Interim reports are provided, ensuring strong interactions with customers.

    In vitro screening
    In addition to in vivo assays, we can perform high-throughput in vitro assays with permanent tumor cell lines (cytotoxicity, cytostasis, cell cycle distribution, apoptosis) as a primary anti-tumor activity screening of your lead compound collections.

    XenTech® proposes fee-for service efficacy studies as well as research collaborations to co-develop theranostics.
  • ALINEA RH - Chargé de Recrutement

    2003 - 2004 ALINEA RH est un cabinet de recrutement spécialisé dans le domaine de la Santé Humaine. Il se compose de 3 départements : Médical, Paramédical et Biotechnologie & Industrie Pharmaceutique
    En tant que responsable du département "Biotechnologie & Industrie Pharmaceutique" j'ai mis en place et géré les bases de données Clients et Candidats, j'étais en charge de la prospection commerciale pour mon département.
    Pour l'activité Recrutement, j'ai travaillé pour une dizaine de clients ( 30 personnes recrutées sur différents postes allant du technicien de maintenance au manager avant projet en cardiologie).
  • MOLECULAR ENGINES LABORATORIES - Ingénieur

    Будапешт 2001 - 2002 Responsable d'une plate forme de PCR en Temps réel pour la mise en évidence de différentiels d'expression de gènes entre une lignée cellulaire tumorale et la lignée n'exprimant plus le caractère tumoral.
    400 gènes étudiés et validés et publiés dans une revue internationale à grand comité de lecture
  • Laboratoire d'Oncologie Médicale - Ingénieur d'études

    2001 - 2001 Mise au point de tests de détection des mutations ponctuelles (SNiPs) dans la séquence génomique des enzymes intervenant dans le métabolisme des xénobiotiques et dans la réparation de l'ADN

Formations

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