Emplois actuels liés à Scientist, Animal Sciences - Pessac Gironde - TreeFrog Therapeutics
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Research Scientist for Solid-State Refrigeration
il y a 3 semaines
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il y a 4 semaines
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Junior Data Scientist Internship
il y a 3 semaines
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Junior Data Scientist Intern
il y a 1 mois
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Junior Data Scientist Intern
il y a 3 semaines
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Scientist - Stem Cell Biology (Kobe, Japan) (H/F)
Il y a 4 mois
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Data Scientist Internship Opportunity
il y a 3 semaines
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Junior Data Scientist Intern
il y a 3 semaines
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Junior Data Scientist Intern
il y a 1 mois
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Data Scientist Internship Opportunity
il y a 2 semaines
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il y a 1 mois
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il y a 3 semaines
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il y a 2 semaines
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il y a 2 semaines
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Data Scientist Internship Opportunity
il y a 1 mois
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il y a 3 semaines
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Scientist, Animal Sciences
Il y a 2 mois
English version below]
#PRÉSENTATION DE L'ENTREPRISE
Treefrog Therapeutics est une biotech innovante dont le but est de rendre les thérapies cellulaires accessibles à des millions de patients, grâce à la technologie C-Stem, qui a été développée pour cultiver et différencier des cellules souches à grande échelle, une 1ère mondiale. Depuis sa création en 2018, Treefrog Therapeutics a levé plus de 74 M€ et connaît une forte accélération grâce à son équipe de plus de 100 collaborateurs.
Contribuer aux études précliniques, y compris la planification, la mise en œuvre, la collecte de données, l'analyse statistique des données, la préparation des rapports et les présentations.
~ Assurer la liaison avec les ORC précliniques pour une planification efficace et une conduite opérationnelle des études DMPK, bioanalytiques et toxicologiques pour les programmes de découverte et de développement, y compris le processus budgétaire/financier ( SOW, PO, factures,...), la conduite de l'étude ( suivi de l'étude toxicologique, gestion des échantillons bioanalytiques...) et l'exécution technique (transfert et gestion des données, rapport d'étude et contrôle de qualité des données...) selon les besoins.
~ Assurer le respect des protocoles d'étude et le suivi en veillant à ce que les études soient réalisées en parfaite conformité avec le protocole d'étude, la certification ISO 9001 ( version de 2015), et la réglementation en vigueur régissant l'expérimentation animale.
~ Etre responsable de la qualité, de la clarté et de l'exhaustivité de la documentation du projet, y compris les dossiers réglementaires.
~ En collaboration avec le responsable préclinique, assurer la communication et le reporting des activités dans le cadre du projet.
Vous êtes titulaire d'un doctorat ou d'un diplôme équivalent en sciences de la vie ou dans un domaine connexe - idéalement en neurosciences, en médecine régénérative, en ingénierie tissulaire -, vous avez minimum 3 ans d'expérience opérationnelle dans le domaine des études précliniques (conceptualisation, organisation et supervision d'études précliniques) et vous avez de l'expérience dans la collaboration avec des sociétés de recherche contractuelle ( CRO). Une bonne connaissance de l'analyse statistique des données et/ou de la gestion de projets serait un atout supplémentaire.
Nous cherchons une personne enthousiasmée par la perspective de déployer les thérapies cellulaires. Vous êtes autonome, organisé(e) et capable de vivre en environnement dynamique dans un projet de longue haleine ? Autonome, bien organisé et méticuleux, vous avez un esprit à la fois objectif et critique.
Maîtrise des outils de gestion de projet
Excellent niveau d'anglais écrit et oral
Autres Avantages :
#Mobilité durable : Nous faisons la promotion d’une mobilité douce grâce à notre partenaire Bee.Plusieurs de nos collaborateurs travaillent ensemble à la réduction de nos déchets et de nos émissions carbones. Nous avons par exemple un frigo connecté zéro déchet.
#Restauration : Nous proposons des tickets restaurant de 9€80 pris en charge à 60% par l’employeur. Contribute to preclinical studies including planning, implementation, data collection, statistical data analysis, report preparation, and presentations.
~ SOW, PO, invoices), study conduct (e.g. toxicology study tracking, bioanalytical sample management), and technical execution (e.g. data transfer and management, study report and data QC) as needed.
~ Ensure compliance with study protocols and monitoring by making sure that studies are carried out in complete compliance with study protocol, ISO 9001: 2015 version certification, and the regulations in force governing animal experimentation.
~ PhD or equivalent degree in life science or related field -ideally in neuroscience, regenerative medicine, tissue engineering-, you have 3 years of operational experience with preclinical studies (conceptualising, organising and overseeing preclinical studies) and you have experience working with CROs. It would be a real bonus to have a good knowledge on statistical data analysis and/or in project management.
Excellent written and oral communication skills in English
