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You will have experience in inflammatory disease, fibrotic and extra-cellular matrix pathobiology, innate and adaptive cell biology and associated in vivo models of disease to join the Gastro-Intestinal Inflammation Research (Drug Discovery Unit.
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Expert in GCDMP, CDISC standards, regulatory compliance (21 CFR Part 11, GDPR), and proficient in MedDRA and WHO-Drug coding, ensuring adherence to ICH GCP and industry standards. Oversee the development and testing of clinical databases and data cleaning procedures, utilizing Medidata Rave/Veeva, and enforce data integrity through comprehensive documentation and quality control.
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By seamlessly integrating semiconductors with conventional microplates, Pixel unlocks multi-modal electrical, electrochemical, and electrophysiological capabilities, delivering an unprecedented scope of data collection and scale-up for cell biology research, drug development, and pharmaceutical manufacturing.
$145,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Be part of a computational team focused on utilizing computational and systems biology approaches to analyze multi-omics data supporting Takeda drug discovery and development projects. Utilize advanced bioinformatics, computational and AI/ML techniques to analyze multi–omics and multi-modal data, identifying novel drug targets and biomarkers, and elucidating molecular and cellular mechanisms of action in Gastroenterology and Inflammation portfolio.
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Hands-on experience in handling, processing, integrating, and analyzing large heterogenous biological data sets related to industrial drug discovery research (e.g., sc/snRNAseq, ATAC-seq, genomics, proteomics, etc.
$166,500 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Provides ad-hoc programming support to Clinical Operations, Data Management, Statistical Programming, Biostatistics, Drug Safety, Clinical Science, Medical Writing and Drug Safety to ensure rapid access to clinical study data for data cleaning/validation, SAS listings review, TLF, dry runs, etc.
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Oversee in vivo and in vitro studies, including development and optimization of disease models, study design, data collection, and interpretation. Develop and validate immunological assays (, flow cytometry, ELISA, CyTOF, cytokine profiling) to evaluate drug candidates' efficacy and mechanism of action.
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Reviews and advises on data, reports, scientific conclusions, and presentationsApproves DMPK components of drug strategy for all (NS, GI2 or ONC) projects at appropriate milestones, reviews and approves the appropriate sections of internal project documentation.
$322,300 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Lead internal and outsourced development and qualification or validation of biomarker assays for clinical trials, applying experience across relevant methods (e.g. qPCR, digital drop PCR, Western blotting), to develop robust assays, generate and analyze data and provide expert interpretation of the effects of promising drug candidates.
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Scorpion has built a proprietary and fully integrated platform of the most advanced technologies across cancer biology, medicinal chemistry, and data sciences, with the goal of consistently and rapidly creating exquisitely selective small molecule compounds against an unprecedented spectrum of targets.
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Knowledge of Government Pricing regulatory requirements and industry leading practices related to Medicaid Drug Rebate Program, Medicare Part B Program, 340B Program, and Veterans Administration Federal Supply Schedule Program pricing and reporting compliance.
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QSP models are mathematical models that are used to integrate knowledge and data on disease pathophysiology and drug pharmacology in a mechanistic manner. Experience with general programming and data analysis tools/languages such as Python, R, Spotfire would be particularly desirable.
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Senior Scientist, Mass Spectrometry, Early Oncology Join our Boston R&D chemistry team as a Senior Scientist, where you'll use your expertise in small-molecule mass spectrometry to analyze a wide range of drug-like small molecules, linkers, payloads, and new modalities using UHPLC-MS techniques.
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Knowledge of Renewable projects (Solar , Wind farm, Hydro and BESS) and data center projects is a strong plus. Proven track record of upholding workplace safety and ability to abide by WSP’s health, safety and drug/alcohol and harassment policies Preferred QualificationsWitnessing and/or performing factory inspections, cable and accessory manufacturing, production and sample tests, type tests and pre-qualification (PQ) and qualification tests.
$189,300 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Leveraging more than 30 years of experience in life science informatics, we are uniquely positioned to deliver a portfolio of innovative BioPharma knowledge management technologies to streamline the capture, analysis, reporting and sharing of data required to accelerate the next generation of life-changing therapies.
$165,000 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago
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