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Qualifications: PhD degree in clinical pharmacology, pharmacy, biomedical engineering, statistics, applied mathematics, or a related field. Knowledge of Health Authority perspective on clinical pharmacology and use of modeling and simulation.
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Job Description Takeda Development Center Americas, Inc. is seeking a Senior Manager, Clinical Data Management in Lexington, MA with the following requirements: Master’s degree in Pharmaceutical Sciences, Pharmacology or Toxicology or related field or foreign academic equivalent plus 6 years of related experience.
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Demonstrates current knowledge of pharmacology and medication administration and reconciliation. Comprised of Tufts Medical Center, Lowell General Hospital, MelroseWakefield Hospital, Lawrence Memorial Hospital of Medford, Care at Home - an expansive home care network, and large integrated physician network.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Strong understanding of all aspects of compound optimization including synthetic chemistry, structure-based drug design, ligand-based drug design, pharmacokinetics, pharmacology, and toxicology.
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The candidate should possess an in-depth understanding of safety pharmacology, investigative and regulatory toxicology, and have experience designing and critically evaluating results of exploratory and GLP-compliant toxicology studies.
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Collaborate with a world class, multidisciplinary team of drug discovery scientists from medicinal and platform chemistry, DEL, in vitro pharmacology, biology, and data science to advance multiple small molecule programs as new clinical candidates for the treatment of several diseases.
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We are looking for a talented and highly motivated scientist to join our in vitro pharmacology group. Manage and/or mentor scientists in the in vitro pharmacology group. Ensure the timely execution of assay development, regular compound screening, HTS campaigns, and data delivery to project teams.
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Knowledge of biotherapeutic structure, pharmacology, disposition and immunogenicity and the impact on assay selection. Design, develop and implement ligand-binding assays (e.g. ELISA, MSD, Gyrolab, PCR) to measure process impurities and/or protein concentration in a fast paced and dynamic environment.
$32 - $40 an hourExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Apply immunology, molecular and cell biology, genetics, and pharmacology know-how to develop and communicate a thorough mechanistic understanding of disease pathogenesis and target rationale. Reporting to the Executive Director, Research, the Director, Immunobiology will drive research activities to design, characterize, and develop therapeutic antibodies as well as support preclinical mechanistic studies of biologic drug candidates for the treatment of autoimmune and inflammatory diseases.
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Takeda Development Center Americas, Inc. is seeking a Senior Manager, Clinical Data Management in Lexington, MA with the following requirements: Master’s degree in Pharmaceutical Sciences, Pharmacology or Toxicology or related field or foreign academic equivalent plus 6 years of related experience.
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Design and develop data capturing tools: Electronic Data Capture (EDC) Systems (Eg: iMedidata Rave and IBM Clinical) eCOA, IRT; Manage electronic Trial Master File (eTMF) QC review eg: Veeva Vault; Lead the Audit and Inspection/Submission Readiness activities like documentation of QC and preparing Storyboards (Eg: FDA/EMA Submissions.
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Head of Medicinal Chemistry and Head of the Novo Nordisk (NN) Small Molecule Research Unit. Will interact and closely collaborate with other Small Molecule Unit Scientists (chemists, biochemists, biophysicists, crystallographers), Data Science & Innovation (DSI) computational chemists, Global Drug Discovery (GDD) biology, Global Research Technologies (GRT), GDD Drug Metabolism and Pharmacokinetics (DMPK), cellular biology, pharmacology and translational medicine teams globally.
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By clicking the Apply button, I understand that my employment application process with Takeda will commence and that. Company headquarters in Lexington, MA. Individual may reside anywhere in the U.S. Up to 100% remote work allowed from any location in the U.S.
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Requires a PhD in immunology, molecular biology, or cell biology plus postdoctoral experience (or equivalent relevant experience) with 10+ years’ industry experience in research or drug development. The Director, Immunobiology will also contribute to the efforts to elaborate mechanistic pathway biology, biomarker discovery, and disease indications.
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The Sr. Scientist will work closely with pharmacology and medicinal chemistry team, lead DMPK efforts to optimize molecules across a variety of therapeutic areas utilizing in vitro, in vivo, and in silico methods and models to generate novel chemical matter with drug-like properties.
Full-timeExpandUpdated 19 days ago
pharmacology job in Wilmington, MA
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