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Previous relevant & significant clinical study experience, across the broad spectrum of Clinical Pharmacology and FIH studies, either in the biopharmaceutical industry leading early phase clinical trials, as a PI or sub-investigator in a CRO or relevant academic medical center.
$257,600 - $386,400 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The incumbent will collaborate with all the groups involved in Clinical Development e.g., Clinical Pharmacology (CP), Clinical Operations, Biometrics, Pharmacovigilance, Regulatory Affairs, HEOR and Medical Affairs.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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In collaboration with AbbVieAbout the Role:Medical expert responsible for the development of clinical research strategies and independent direction of Phase 1-3 clinical studies while working with cross-functional project teams (clinical project managers, research, preclinical/clinical pharmacology, biometrics, regulatory, drug safety, CMC), creation and execution of clinical development plans, and the development of strategies that will ultimately lead to approvals of Neurocrine's products.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Amador Bioscience (AmadorBio) is a Translational & Clinical Pharmacology CRO providing global-standard services in quantitative clinical pharmacology, GLP/GCLP bioanalysis, clinical research, and regulatory filing to leading biopharmaceutical companies.
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Gilead Sciences is a biopharmaceutical company that discovers, develops and commercializes innovative therapeutics in areas of unmet medical need. At least 8 years' experience and a, PhD, PharmD or MD degree with emphasis in clinical pharmacology, pharmacokinetics or a related scientific discipline.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The Toxin Innovation Pharmacology Group at AbbVie is seeking a Principal Scientist who is highly motivated and innovative, and possesses strong leadership and communication skills to lead a neuromuscular junction in vivo research team.
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It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
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Qualifications (Minimal acceptable level of education, work experience, and competency) · PhD (or equivalent) in biological sciences including molecular/cell biology, pharmacology, or biochemistry with focus on immunobiology.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Extensive experience and strong understanding of biopharmaceutical drug development, the competitive landscape / oncology market dynamics / evolving treatment landscape and HCP and patient insights, bringing deep clinical and external stakeholder insights to decision making from pre-POC to post-POC and commercialization.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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PhD in Pharmacokinetics, Pharmacology, Pharmaceutical Science or other relevant field with 15+ years of experience in the biopharmaceutical industry. Design and execute preclinical studies to understand the pharmacokinetics (PK) and absorption, metabolism, distribution, and excretion (ADME) of drug candidates that support drug discovery, preclinical and clinical development.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Represent and provide clinical pharmacology expertise and leadership at cross-functional development project team, clinical subteam, study team, partnering with clinical research, biometrics, project management, clinical operations, drug metabolism, biology/biomarkers, toxicology etc.
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A PhD in toxicology, pharmacology, biology, or equivalent scientific discipline is required, with a minimum of 8-10 years of relevant research experience in a pharmaceutical or biopharmaceutical setting.
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Strong knowledge of pharmacokinetics and modeling, pharmacodynamic principles, ADME concepts, bioanalytical principles, regulatory guidelines and clinical pharmacology requirements in late stage clinical development.
$220,000 - $240,000 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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PhD or PharmD in Pharmaceutical Sciences, Pharmacokinetics, Pharmacometrics, Engineering, or related scientific discipline, with 10+ years of relevant biotech/biopharmaceutical experience. The Company is seeking to hire a Director, Quantitative Pharmacology within the Quantitative and Clinical Pharmacology sub-function in Development Sciences to develop and execute modeling and simulation (M&S) strategies supporting preclinical translational pharmacology efforts and all stages of clinical development.
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Mosaic teams provide comprehensive, end-to-end discovery services, including program assessment and strategy development; program management; antibody discovery and optimization; protein production, purification, and characterization; protein engineering; biochemical and cellular assay development; formulation, stability and developability studies; bioanalytical (PK and PD) assay development; and candidate-validating pharmacology.
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