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Strong writing, editing, proofreading, layout and design, professional printing/publishing skills are essential, including ability to present concepts verbally. Video editing, basic graphic design and website design skills using tools such as Canva and Adobe Suit are preferred.
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Beam is seeking an Associated Director / Director, Patient Supply who will provide leadership, planning, and execution of clinical supply activities to support the Beam Therapeutics in-vivo gene editing clinical program.
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This individual will design and execute experiments that leverage rare-disease patient datasets, large-scale human genetic datasets (e.g. UK Biobank), catalogs of disease mutations (e.g. OMIM, ClinVar), and molecular data (e.g. RNA expression, proteomics) to understand the genetic etiology of severe diseases; identify therapeutic mechanisms amenable to Editas' gene editing strategies; and characterize patient populations amenable to treatment.
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And genomic techniques (CRISPR/Cas based gene editing). PRINCIPAL DUTIES AND RESPONSIBILITIES Establish procedures for tissue culture-based experiments that involve measuring different phenotypic readouts (RNA, protein, reporter, viability, etc.
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HSCRB faculty members’ research spans broad areas of science, including but not limited to: developmental biology; regeneration and aging; neurobiology; systems biology; development of novel technologies and therapeutics (e.g. -omics, gene editing, gene therapy); stem cell biology; and genetic and biochemical mechanisms of disease.
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As a member of the Process and Analytical Development (PAD) department, the Senior Development Associate contributes to Editas’s efforts to develop safe and effective cellular therapies using CRISPR-based gene editing technologies.
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In this role you will be a critical member of a team responsible for establishing and integrating state of the art chemical proteomics technologies and workflows across all functions within the protein editing platform.
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The ElevateBio ecosystem combines multiple R&D technology platforms – including Life Edit, a next-generation, full-spectrum gene editing platform; comprehensive cell engineering technologies; and an expanded viral and non-viral therapeutic delivery platform – with BaseCamp®, its end-to-end genetic medicine cGMP manufacturing and process development business, to accelerate the discovery and development of advanced therapeutics.
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Additionally, the candidate will be tasked with submitting release reviews, creating and maintaining spreadsheets, running LLBIS (Lab Financial Reporting System) reports, drafting and editing presentations, preparing and recording Group TEAMS meetings, and supporting security audits.
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Conduct formulation and/or process screening to improve biophysical characteristics and in vivo gene editing in animal models. The Scientist will work on developing safe and potent delivery systems to enable in vivo gene editing.
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The Head of Product Sciences role is situated within the larger CMC organization responsible for process development, analytical development, technology transfers, manufacturing, and supply of our drug product TCR T cell candidates, drug substance and critical intermediates such as gene editing reagents, viral (LVV) and non-viral vectors.
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The Scientist I, Bioinformatics is part of the Genomics and Data Sciences team and plays a critical role in supporting Discovery Biology to advance our portfolio of RNA, gene therapy, and CRISPR-based gene editing therapies to treat neuromuscular and CNS-related disease.
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Work closely with representatives from different therapeutic areas, as well as those from Editing Technologies, Tissue and Cellular Imaging, Genomics and Computational Biology, Pharmacology, Toxicology and Program Management groups to coordinate workflows.
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Understanding of Adobe Creative Suite (especially InDesign) for editing and design of marketing materials is a plus. The selected candidate will gain an understanding of the full range of economic development programs offered by the City. The selected candidate will be responsible for a wide variety of tasks with a focus on community engagement to small businesses and/or startup companies (this includes both in-person outreach and development of materials), open data development, cross-departmental planning efforts, event management, and other areas as needed.
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The scientist will work on optimization of lead LNP formulations to enable safe and potent in vivo base editing. Lead the design and execution of experiments to optimize LNP composition and process to improve in vivo base editing.
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editing job in Lexington, MA
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