Post Doctorant Pharmacologie

OverviewJoin to apply for the Post Doctorant Pharmacologie (organoïde et in vivo) role at Ipsen.What - Summary & Purpose Of The PositionThis postdoctoral position aims to design, develop, and evaluate disease-relevant in vitro 3D models (organoids/spheroids) to strengthen predictive pharmacology and biomarker translation for clinical success. The role will benchmark new approach methodologies (NAMs) against existing 2D and in vivo models, consolidate data across CRO partners, and bridge findings with in vivo PDX/mini-PDX studies to assess translational value. The postdoc will operate across Paris HQ and Dreux labs and collaborate with selected CROs to ensure robust methodology, reproducibility, and alignment with FDA/EMA guidance on alternative methods. Expected impact includes increased relevance of preclinical models, reduced animal use where scientifically justified, and improved decision-making for Ipsen’s pipeline.What - Main Responsibilities & Technical CompetenciesMain ResponsibilitiesInnovate With 3D ModelsDevelop and characterize organoid and spheroid models to better predict drug response and biomarker behavior either with external collaboration with CROs or in our internal lab facilities in DreuxBridge In Vitro And In VivoPlan and conduct in vivo studies in CROs (PDX, mini-PDX) to validate translational potential and establish correlations with 3D models.Drive Scientific ExcellenceDesign protocols, ensure data quality and analysis.Document experimental protocols and results in compliance with Ipsen standards and quality; Record data in ELNs and write reportsEnsure compliance with ethical and regulatory standards, and deliver robust, reproducible data packages.Stay up to date with emerging technologies and scientific advances in NAMs.Collaborate And CommunicateWork closely with CROs, internal teams, and academic partners. Present findings and strategic recommendations to Ipsen’s Translational Sciences team.Collaborate with translational teams to integrate findings into clinical biomarker strategies.Collaborate with in vitro pharmacology and clinical biomarker teams.Communicate results effectively in multidisciplinary project meetings and external conferencesParticipate to external communication and/or publication (if applicable)Technical CompetenciesHands-on experience with 3D models (organoids, spheroids) and in vivo models (oncology, PDX).Strong technical skills: imaging, qPCR, IHC, multiplex assays, PK/PD analysis.Knowledge of NAMs and regulatory guidelines (FDA/EMA).Excellent communication skills and fluency in English.Familiarity with translational research and biomarker development.Behavioural Competencies RequiredScientific curiosity and innovation – ability to propose and implement novel approaches.Collaboration and communication – team player working effectively in cross-functional teams.Problem-solving and adaptability – manage complex experimental challenges.Accountability and rigor – ensure high-quality, reproducible researchCompliance with Environment, Health, and Safety (EHS) regulations and proceduresContribute to the site's EHS performance by reporting risks, malfunctions, or improvementsParticipate in mandatory EHS trainingBehavioural Competencies RequiredCollaboration – e.g., working closely with CROs and internal teams to align project goals.Accountability – taking ownership of experimental design and data integrity.Agility – adapting to new technologies such as organ-on-chip platforms.Innovation – proposing novel approaches for predictive pharmacology.Integrity – ensuring compliance with ethical and regulatory standards.Knowledge & Experience (essential)Experience in designing and performing in vitro and ex vivo models 3D models.Expertise in cell culture methods, cellular and molecular biology and biochemistry.Experience in designing and piloting in vivo studiesAble to develop new techniques and methodologies tailored to project needsExposure to translational activities linking preclinical findings to clinical applications.Good organizational and prioritization skills.Ability to work as part of a team in a multidisciplinary environment in a matrix environmentStrong problem-solving and critical thinking abilities.Excellent communication and collaboration skills (written and oral).Travel to Dreux as required for lab experiments, projects and interaction with TS team members.Knowledge & Experience (preferred)Familiarity with new approaches for 3R and clinical trial support.Education / Certifications (essential)Ph.D. in Pharmacology, Oncology, or related field.Language(s) (essential)French fluentFluent EnglishSeniority levelNot ApplicableEmployment typeFull-timeJob functionResearch, Analyst, and Information TechnologyIndustriesPharmaceutical ManufacturingNotes: Referrals and external postings are not required to assess the candidate; dates and locations reflect posting history and do not impact role responsibilities. #J-18808-Ljbffr