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Validated ability to synthesize information from multiple scientific fields to generate insights to guide product design and development - analytical & physical characterization, in-vitro & in-vivo model systems, PBPK modeling, sensory psychophysiology, consumer research, etc.
$112,800 - $163,500 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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PhD in pharmacokinetics, chemistry, biochemistry, or a related scientific discipline. The Associate Director, PK and Bioanalysis at Pharmaron, will play a pivotal role in directing the scientific aspects and processes of in vivo pharmacokinetic studies, inclusive of bioanalysis and comprehensive reporting of noncompartmental PK parameters.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Ability to synthesize, interpret and integrate diverse, multidisciplinary scientific data (e.g., pharmacology, pharmacokinetics, pathology). Maintains a current understanding of relevant literature and methodology, as well as the scientific literature related to the assigned Jazz pipeline products and R&D projects.
RemoteExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Develops and demonstrates the ability to perform pharmacotherapy, pharmacokinetics consultations and other clinical. Performs the basic Pharmacist procedures required by the assigned area consistent with scientific principles and Orlando Health policy and procedures.
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Good knowledge of statistics and drug development processExperience as a lead programmer for NDAs/BLAs. Experience overseeing the work of internal contractors and external vendors (CROs)Experience in pharmacokinetics/pharmacodynamics modeling a plusFamiliarity with CDISC standards, including SDTM and ADaM modelsSolid verbal and written communication skillsFOR US-BASED CANDIDATES ONLY.
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Strong scientific understanding of non-clinical in vivo pharmacology evaluation. · Lead the design, conduct and interpretation of nonclinical in vivo studies to support pharmacology, pharmacokinetics/biodistribution, and safety assessments.
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Authors work orders when necessary QualificationsQualificationsMust be recognized applied development practitioner, experienced in both design and stewardship of clinical pharmacology components of clinical development plans and optimal application of pharmacometrics approaches to support decision making and regulatory successPhD or PharmD degree or equivalent degree with specialization in pharmacology or pharmacokinetics, or in a related scientific discipline.
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Job Field: Pharmacokinetics & PharmacometricsOrganization: Janssen Research & Development, LLC (6084) Stay abreast of clinical pharmacology, MIDD, analysis methodology and overall drug development process, including regulatory guidance, and methods in modeling and simulation by engaging with the scientific community (e.g., publishing, presenting at meetings, participating in special interest groups within professional societies, etc.
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PhD or PharmD degree or equivalent degree with specialization in pharmacology or pharmacokinetics, or in a related scientific discipline. MS in Pharmaceutical Science with job related experience in the field of drug development and clinical pharmacology.
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Provide oversight to the development of Model Informed Drug Development (MIDD) plans, involving planning and execution of quantitative analyses which may include population pharmacokinetics, pharmacokinetics (PK)/pharmacodynamics (PD), exposure response, disease progression modeling, model-based meta-analysis, and decision analysis.
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At least 3 - 5 years of basic or clinical research experience in an academic or industrial setting, with experience in analysis of research data and publications; working knowledge of biostatistics and pharmacokinetics; working knowledge of Good Clinical Practice, scientific and clinical research methods and clinical study design.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Responsibilities:We are currently seeking a Director, Drug Metabolism and Pharmacokinetics, who will have scientific oversight of one or more of the small molecule discovery projects and will manage the in vitro and in vivo PK, ADME and bioanalytical assays.
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The Associate Director, External Research, Scientific Affairs provides strong subject matter expertise, operational oversight and process requirement support for the intake, evaluation, documentation, execution and follow-up of External Research (ER) activities, such as Investigator Initiated Studies (IIS) and External Collaborative Research (ECR.
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Good knowledge of statistics and drug development processExperience as a lead programmer for NDAs/BLAsExperience overseeing the work of internal contractors and external vendors (CROs)Experience in pharmacokinetics/pharmacodynamics modeling a plusFamiliarity with CDISC standards, including SDTM and ADaM modelsSolid verbal and written communication skills.
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Strong quantitative experience (e.g., pharmacometrics, pharmacokinetics/pharmacodynamics, quantitative systems pharmacology, statistics) Supporting Pfizer Oncology, you will be a senior scientific and strategic leader and a member of the Pharmacometrics and Systems Pharmacology Leadership Team. In this key role, you will influence the discovery and development of drugs and expand the application of model-informed drug development (MIDD) approaches within oncology and across our portfolio.
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