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We're looking for someone exceptional to join our growing team as an Associate Scientist in the In Vivo Pharmacology group. Perform in vivo studies including drug administration and assessing in vivo pharmacology.
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The In Vivo Pathology (IVP) team within the Pathobiology department is seeking a research associate to contribute to histology and pathology workflows in support of pre-clinical in vivo pharmacology studies.
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Be a thought partner providing scientific input for in vivo preclinical toxicology studies. PhD + 5 years' experience in toxicology or other closely related life sciences field, in the industrial or CRO setting, executing, or managing in vivo studies for the purpose of advancing a biological therapeutic candidate into the clinic (BS +11 years or Masters + 9 years will also be considered.
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Our Research & Development Division located in South San Francisco is seeking an Associate Principal Scientist with strong expertise in complex cellular model/assay development, mechanistic receptor pharmacology, and lead discovery to join our Quantitative Biosciences (Pharmacology) department.
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Cell biology and engineering: e.g. cell culture, flow cytometry, confocal microscopy Molecular biology and engineering: e.g. plasmid cloning, CRISPR Animal studies with rodents: e.g. transplantation, survival surgery, in vivo imaging.
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The Executive Director of Neuroscience In Vivo Pharmacology and Translational Biomarkers is responsible for leading a group tasked with all aspects of generating in vitro and in vivo data used to develop pharmacokinetic / pharmacodynamic relationships, and the identification of translational biomarkers to support lead optimization and clinical development of PROTAC degrader molecules for severe neurologic disorders.
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Extensive hands-on experience building quantitative in vitro assays (biochemical and cellular) and expertise with in vivo pharmacology models in an oncology drug discovery setting.
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Our pathologists are empowered by access to AI digital pathology, multiplex assays, advanced molecular imaging techniques, and a full suite of in vivo imaging technologies. Are you a passionate veterinary anatomic pathologist interested in driving innovation in drug discovery to bring safe and effective therapies to cancer patients.
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They will interact daily with our data science and computational group for interpretation and design, our biology and pharmacology group to develop assay workflows for in vivo translation, and our chemistry group to push the boundaries of what is possible with parallel chemistry and library syntheses.
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Experience with in vitro and in vivo pharmacology studies, e.g. sterile cell culture techniques, and rodent handling experience (animal dosing (IV, PO, IP, SC), tumor implantation, blood/tissue collection, etc.
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At 1910 Genetics, we put computation at the heart of drugdiscovery, blending expertise in computational chemistry, structuralbiology, pharmacology, genetics, data science, and softwareengineering to develop drugs for previously undruggable targets.
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Establish in-vitro and in-vivo screening capabilities for lead optimization and lead nomination. Build long-term, collaborative relationships with key experts in the rare disease and Peptide/Oligonucleotide field.
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Ampersand is currently seeking an experienced leader with deep expertise in drug development to head our In Vivo Pharmacology team. The ability to collaborate closely with the leadership team and other R&D leaders while guiding the in vivo pharmacology team to achieve the company's objectives is an essential element of the role.
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This individual will lead the in vivo pharmacology efforts to drive discovery to identify new lead molecules, and design and execute mechanistic studies to characterize these compounds and their impact on physiology and pathophysiology.
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Effective cross-functional collaboration, especially with Institutes of Science, In Vivo Pharmacology and DMPK, in the optimization of drug leads and candidates. Strong knowledge and agility in study design and data interpretation and in the integration of Toxicology studies in the drug progression paradigm, as well as in the incorporation of safety endpoints in pharmacology studies.
$265,200 - $439,300 a yearFull-timeExpandApply NowActive JobUpdated Today
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