• Associate Director , Clinical

    J&J Family of Companies (Raritan, NJ)
    Associate Director , Clinical Pharmacology and Pharmacometrics - 2306103445W **Description** Janssen Research & Development, LLC is recruiting for an ... Associate Director , Clinical Pharmacology and Pharmacometrics (CPP) to be located in Spring House, PA, Titusville, NJ or Raritan, NJ. At the Janssen… more
    J&J Family of Companies (03/25/24)
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  • Associate Director , Clinical

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    Associate Director will be responsible for developing and implementing Clinical Pharmacology and Modeling & Simulation plans from FIH to post ... registration. Responsibilities include the development of Clinical Pharmacology and Modeling and Simulation plans, design and lead study teams to execute … more
    Daiichi Sankyo Inc. (04/23/24)
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  • Associate Director , Quantitative…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …immune disorders. **Summary** The Associate Director , Quantitative Systems Pharmacology (QSP) will work within the Quantitative Clinical Pharmacology ... which include target prioritization, therapeutic modality selection, biomarker characterization and clinical trial design. In addition, he/she will develop a QSP… more
    Daiichi Sankyo Inc. (04/23/24)
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  • Associate Director , Clinical

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …responses to IRBs and Health Authorities; Collaborates with Translational Medicine and Clinical Pharmacology to ensure appropriate biomarker, PK / PD ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs.… more
    Daiichi Sankyo Inc. (04/19/24)
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  • Associate Director , Clinical

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …responses to IRBs and Health Authorities; Collaborates with Translational Medicine and Clinical Pharmacology to ensure appropriate biomarker, PK / PD ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs.… more
    Daiichi Sankyo Inc. (03/21/24)
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  • Associate Director PKDM

    Sanofi Group (Bridgewater, NJ)
    …complex issues at various stages of drug development. + Responsible for clinical pharmacology contributions to regulatory documents and inquiries. + Interfaces ... **Basic Qualifications** + Minimum 5 years of experience in clinical PK/PD, pharmacometrics, and/or clinical pharmacology...of experience in clinical PK/PD, pharmacometrics, and/or clinical pharmacology + Proficient in PK modeling… more
    Sanofi Group (05/09/24)
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  • Associate Director , Informatics

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    Clinical Development, Biostatistics and Data Management, Regulatory Affairs, Quantitative Clinical Pharmacology , Clinical Safety and Pharmacovigilance, ... Regulatory/Risk Management, Quality Assurance, Medical Affairs, Translational Research, Research, Informatics Services, Project Management and Operational Management. Develop a strong, positive strategic business partnership with the global R&D business and… more
    Daiichi Sankyo Inc. (05/12/24)
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