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Seeking a highly motivated flow cytometry scientist to join theFlow Lab team in managing the day-to-day activities of the Flow Cytometry Core Lab. This position requires advanced technical expertise and the ability to provide highly complex multi-parameter flow cytometry and multi-dimensional sorting support to Discovery, Translational, and Clinical research in Oncology.
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Your main responsibilities as a Senior Research Associate, Formulations:Execute experiments for the formulation and QC of oral and parenteral vehicles for in vivo evaluation of novel lead materials.
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Perform cell culture procedures, including culture of primary cells, flow cytometry, single cell analysis methods, and possibly other techniques. Join a culture of revolutionary research that is looking to eradicate HIV. This position is funded and hired through NCIRE- The Veterans Health Research Institute, which is affiliated with the San Francisco VA Medical Center and the University of California, San Francisco (UCSF.
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This laboratory-based role involves close collaboration with colleagues and teams across multiple functions including cell therapy, molecular biology, protein engineering, computational sciences, functional genomics, in vivo pharmacology, early clinical development and manufacturing.
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Preferred Experience Proficiency in qualitative research methods (e.g., interviews, expert consultation, case studies). Our primary offerings include: Program Design and Strategy DevelopmentProgrammatic Research, Analysis, and ModelingGrant Support: Sourcing, Conducting Due Diligence, Making Grant Recommendations, Grantee ManagementProject Incubation, Nonprofit Business Planning, Organizational Development, and Staffing SupportEvaluation and LearningFacilitation, Collaboration, and Grantee ConveningRecruiting and Organization Design About the RoleCEA is looking for a Research Associate.
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Grow and lead the In Vivo Pharmacology team in performing critical preclinical PK-PD and efficacy studies across different therapeutic areas. In depth in vivo pharmacology experience, particularly in the design and execution of rodent disease models across therapeutic areas.
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Founded by CRISPR pioneer and Nobel laureate Jennifer Doudna and Trevor Martin, Janice Chen, and Lucas Harrington, the company's ultracompact proteins are designed to enable in vivo gene editing in difficult to reach tissues utilizing both nuclease applications and new editing modalities beyond double stranded breaks, including base editing, gene writing, and epigenetic editing.
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Develop and enhance complex in vitro and ex vivo research and development capabilities. Proficiency with cell-based assays, ELISA, MSD, qPCR, RNseq, microscopy, histology/pathology (e.g., IF/IHC/ISH), and/or flow cytometry.
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Name recognition of bulge bracket broker research firms and major U.S. At least 2-5 years experience in related research. Be well versed in Factset, Refinitiv, S&P, CapIQ, Factiva, Westlaw, IHS, MergerMarket, Bloomberg, Dealogic and other data bases.
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Other responsibilities may include utilizing nonclinical PK and PK/PD data (including use of modeling and simulation techniques) to project optimal clinical dosing regimens, doses based on pharmacological/clinical targets, human starting doses, and biomarker exploratory data (including biochemical and molecular data from quantification of mRNA, multi-panel flow cytometry, and protein expression) This position is Hybrid based and travel to our San Francisco office on a regular basis.
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Expertise in independently leading lab-based research projects involving a wide repertoire of experimental techniques such as conventional/spectral flow cytometry, biochemistry, cell/molecular biology, and immune function assays.
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Qualifications:· Candidates should have a doctoral degree in bioinformatics, computational biology, statistics, data science, other relevant fields with at least 1-3 years/ master’s degree with at least 5-7 years/BS degree with at least 10 years of relevant post-degree experience, preferably in pharma/biotech or related research organizations/academia.
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Understanding of general in vivo AAV pharmacology and toxicology best practices. The Study Manager will work cross-functionally with internal program teams and CROs. Responsibilities Primarily responsible for selecting, contracting, and monitoring non-GLP and GLP nonclinical studies with Contract Research Organizations (CROs), expert consultants and academic collaborators.
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Working Title : Clinical Research Coordinator I - Obstetrics & Gynecology - Maternal-Fetal Medicine (Part-Time, Hybrid) The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
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Opportunity Information Clinical Research Coordinator – Interventional Endoscopy San Francisco, CA Sutter West Bay Medical Group Opportunity Information The distinguished Paul May and Frank Stein Interventional Endoscopy Center is the premier referral center in Northern California and the greater region for patients requiring complex endoscopic therapy.
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vivo flow research jobs Company: Adcentrx Therapeutics in South San Francisco, CA
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