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Founded in 2015, the company has built a portfolio of 30+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.
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The Preclinical pharmacology team works closely with the Medicinal Chemistry, High Throughput Screening and Protein Engineering modules. Preclinical pharmacology informs how drug candidates will behave in humans.
$109,000 - $129,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Support in vivo pharmacology studies for ADCs. Support in vivo pharmacology studies for ADCs. We use data science, genomics, synthetic biology, and automation to discover potent, evolutionarily refined small molecules and their cognate targets from fungal genomes.
$120,000 - $180,000 a yearFull-timeExpandUpdated Today - UpvoteDownvoteShare Job
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Oversee and provide strategic direction for Toxicology/Pathology, BioAnalytical/DMPK, Biomarkers, and Clinical Pharmacology teams to ensure robust support for clinical development programs. 12+ years of experience in the biopharma industry in non-clinical development (toxicology, pharmacology, pharmacokinetics, bioanalytical sciences, or related discipline.
$265,000 - $300,000 a yearFull-timeExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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The individual will define and implement preclinical and clinical translational and biomarker strategies for product candidates entering clinical development and execute these strategies in first-in-human clinical trials.
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Conduct nonclinical development activities (pharmacology and toxicology) for IND-enablement of gene therapy products. Design, manage and conduct nonclinical hands-on studies (GLP and non-GLP) for inclusion in regulatory submissions, including pharmacology, toxicology, and biodistribution studies.
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Palo Alto office of a BCG Attorney Search Top Ranked Law Firm seeks life sciences patent associate attorney with 1-4 years of patent prosecution law firm experience, Patent Bar membership, and a background in one of the following fields: cell or molecular biology, immunology, biochemistry, bioinformatics, organic chemistry, medicinal chemistry, cancer biology, pharmacology, biophysics, or digital health-focused disciplines.
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Demonstrated in-depth knowledge of drug development, from preclinical to late-stage development, including experience submitting BLAs and MAAs to the FDA and EMA. Lead one or more Program team comprised of functional representatives from Research, Regulatory, Technical Operations, Clinical Development, and Commercial from preclinical candidate selection through approval and launch.
$260,000 - $360,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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PhD in cell biology, immunology, pharmacology, molecular biology or a closely related field with 0-3 years of industry experience or a B.S. with a minimum of 6 years of industry experience. Significant laboratory experience is required with the ability perform flow cytometry of primary murine and human cells, ELISA, and MSD.
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Disease model screening and extensive preclinical validation to mine stem cell secretomes as a rich source of new medicines for chronic and rare diseases. disease model systems in an intimate and small team focused on the discovery, preclinical validation, and clinical translation of novel biologics for chronic and rare degenerative diseases.
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Design, execute, and analyze preclinical research studies focused on engineering stem cells, and spanning molecular biology and cell biology. Experience with multi-color flow cytometry, panel design, primary cell culture, cell sorting and/or data analysis is preferred.
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Reporting to the Executive Director, Clinical Quality Assurance, the Associate Director/Director, Clinical Quality Assurance will define and support the quality oversight and management of GCP activities internally at BBGT (and other affiliates as directed) and externally with BBGT vendors, consultants, and service providers, including, but not limited to, quality systems management, document review, and approval.
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G., clinical operations, regulatory, preclinical, project management, quality, CMC, etc.) G., Medidata Rave, InForm, etc.) Experience in all aspects of protocol conduct, both early and late phases, including protocol writing, start-up, study execution, analysis, and reporting Sufficient content expertise to be able to meaningfully contribute to document development and data review and interpretation under the direction and oversight of the CMO. Knowledge of applicable FDA Code of Federal Regulations, Good Clinical Practices, and clinical trials guidelines is required.
$250,000 - $315,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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M.D. or Ph. D. degree in Behavioral Neuroscience, Pharmacology, Bioanalytical Neurochemistry, Experimental Psychology, or a related discipline with an established record of independent research aligned with the goals of the Metabolic and Mental Health Program.
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We are seeking a highly motivated and energetic individual with relevant scientific background to be part of the Nonclinical Development and Clinical Pharmacology (NDCP) Organization. Responsibilities:As a key member in Clinical Pharmacology and Pharmacometrics, you will:Provide strategic insight and technical leadership within the Clinical Pharmacologyand PharmacometricsLead the design and execution of an integrated clinical pharmacology and modeling and simulation strategy to guide the clinical development plan.
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pharmacology preclinical jobs in Stanford, CA
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