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The Research Associate 1, In Vivo Pharmacology, will be responsible for maintaining inventory, prepping for experiments, and providing experimental support for preclinical in vivo experiments.
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Expertise in developing and utilizing in vivo mouse models for preclinical evaluation. Employ in vivo mouse models for preclinical evaluation of candidate therapies. Lead the design, development, and optimization of T-cell candidates using in vitro and in vivo assays.
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Stanford Center for Innovation in In vivo Imaging (SCi3) is a shared preclinical imaging facility that provides instrumentation, strategies, expertise, and software tools to perform multimodality in vivo imaging and quantification.
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Key Responsibilities: Lead preclinical studies that provide scientific rationale for advancement to human trials, including safety, efficacy, and mechanisms of action studies using clinically relevant in vitro and in vivo models.
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The Senior Technician will execute experiments, and will also be responsible for performing or collaborating in vivo PK/PD studies done in preclinical models including ex vivo assays (i.e. ELISA based PD read outs.
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We are a recently established translational leukemia research laboratory that uses a variety of biochemical, molecular, and cell biology approaches to identify new therapeutic targets, develop preclinical models of disease, and test novel therapeutics both in vitro and in vivo using mouse models.
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About ASET West Jefferson, OH : AmplifyBios safety, efficacy, and toxicology unit (ASET) was launched as a preclinical CRO that spun out of Battelle in 2021 to address the changing needs of commercial organizations developing modern therapeutics.
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A successful candidate will have had experience with preclinical drug discovery including immunoassays, flow cytometry, cell cytotoxicity assays, and ex vivo cell-based assays. Must be able to work independently and have an understanding of the preclinical drug discovery process.
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Associate Scientist-Oncology (In Vivo Pharmacology) In vitro work includes a range of cellular assays, including multi-parametric flow cytometry and molecular biology techniques to help interpret in vivo observations.
$98,093 - $114,246 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
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The individual will be an integral team member and contribute to the understanding of molecular and cellular phenotypes of in vitro and in vivo models of neuromuscular diseases, discovery and characterization of potential therapeutic compounds using relevant models.
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Perform analysis of in vitro and in vivo editing outcomes using next-generation sequencing, quantitative PCR, and RNA sequencing. We are seeking a Scientist II/Sr. Scientist to evaluate novel genome editing systems for in vivo therapeutics as a member of our growing pre-clinical research team.
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Be a thought partner providing scientific input for in vivo preclinical toxicology studies. The Toxicologist will collaborate with external vendors, the internal preclinical pharmacology and toxicology team, and other stakeholders across the company to ensure efficient processes that scale with Verve's continued growth.
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The Preclinical Therapeutics Core is recruiting a new animal technician to meet the demand for in vivo studies. In addition to animal works, the technician will work closely with Preclinical Therapeutics (PTC) Lab Manager to plan and organize lab operations and weekly schedule.
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The Study Director, Research Scientist will have a passion for preclinical research. Three years’ experience as a Study Director for in vivo studies (including GLP) in a biopharmaceutical company or Contract Research Organization (CRO) One to two years’ experience in Toxicology a plus.
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