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PhD (or M.S. with relevant experience) in Computational Biology, Bioinformatics, Biophysics, Physics, Computer Science, Statistics, Molecular Biology, Genetics, or related discipline. Conversant in molecular biology and genetics, preferably with knowledge of cancer genomics and tumor biology.
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PhD in Chemistry, Biochemistry, Biology or a closely related science with experience in microbial genetics, gene editing, and synthetic biology. Do you have at least a PhD in Chemistry, Biochemistry, Biology or a closely related science with experience in microbial genetics, gene editing, and synthetic biology.
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Biomedical Science content areas will include anatomy, genetics, physiology, biochemistry, histology, microbiology, immunology, pharmacology and neurosciences, as well as other biomedical sciences and clinical sciences.
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PhD and/or MD with expertise in molecular genetics, human genetics, molecular pathology or related field. Ambry Genetics Corporation is a CAP-accredited and CLIlicensed molecular genetics laboratory based in Aliso Viejo, California.
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Position Information: Lee Physician Group (LPG) Pediatrics is seeking a full-time ABMGG Board Certified/Board Eligible Medical Geneticist to join their team, which is currently lead by Jeffrey W. Innis, MD, PhD (jeffrey.innis@leehealth.org.
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Education: PhD in the Life Sciences required (Cell Biology, Molecular Biology, Genetics, Immunology, Biochemistry preferred. Must have training relevant to cell therapy, stem cells, CAR-T cells, cell culture, flow cytometry and cryogenics.
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PhD in Genetics, Molecular Biology, Biochemistry or related discipline earned within the last two years. Mouse genetics experience and familiarity with NGS is desired but not essential.
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MS or PhD in Biological Sciences, Biomolecular Engineering, Biochemistry, Molecular Biology, or a related field, with 5-8+ years of relevant experience in a commercial diagnostics and assay development laboratory.
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PhD in Pharmacology and/or PharmD with a minimum of 6+ years of drug development industry experience specifically in clinical pharmacology, pharmacometrics and/or modeling and simulations. Maze Therapeutics is a biopharmaceutical company that is harnessing the power of human genetics to transform the lives of patients, with a focus on genetically informed therapies for common diseases such as chronic kidney disease.
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PhD degree in genetics or statistics or computational biology or computer science. The Section of Genetic Medicine conducts impactful investigations focused on quantitative genetics, systems biology and genomics, bioinformatics and computational biology.
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PhD in a biological science related field (Pharmacology, Genetics, Biochem etc.) Understanding of standard drug development process, defining in vivo pharmacology, assessing PKPD and deriving margins to provide clinical starting doses.
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PhD (and/or MD) or similar degree in molecular biology, cell biology, genetics, neuroscience, or related field. Ambitious, driven candidates with a recent PhD (and/or MD) in molecular biology, cell biology, genetics, neuroscience, or related field with a solid thesis publication record are encouraged to apply.
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Design, implement, analyze, and report findings from targeted statistical research studies; provide consultation and guidance to researchers on experimental design, statistical research methodologies, and scientific standards for in vivo/in vitro studies, asay development, biomarker researches, and genetics/omics data analyses etc to advance drug development research.
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Qualifications Minimum Qualification: Successful completion of a PhD from an accredited college with a degree in fisheries science, conservation genetics, or conservation genomics. The focus of EESC-LRL mission and vision for the future is to continue its dynamic international, national, and regional leadership in aquatic, landscape, and genetics research by generating, interpreting, evaluating, and transmitting the scientific information needed to better address the pressing problems of managing our nation's biological resources, especially those under the stewardship of the Department of the Interior, and other Federal and non-Federal partners.
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Collaborate with In Vivo Pharmacology and DMPK on development of translational PKPD models. Develop and integrate timelines and budgets for clinical pharmacology activities with overall company timelines and goals, in close coordination with project management, clinical science, CMC, DMPK, nonclinical development, regulatory affairs and other stakeholders.
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