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This process involves closely collaborating with scientists across the organization to support the overall safety assessment for our novel therapeutics spanning drug discovery through clinical development and marketing.
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As a vital part of their research team, this scientist will lead the design, implementation, and optimization of cutting-edge deep learning models tailored to the unique challenges of drug discovery.
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This includes but is not limited to responsibility for genomics and gene expression profiling (GEP) biomarker assay technology/ platform selection, evaluation of in-house or vendor choice per assay use requirements, development, optimization, qualification/validation and/or execution of biomarker analysis for BMS translational medicine and clinical programs.
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Consultation responsibilities may include questions related to clinical care, research study design, international ethics, and other bioethics topics relevant to the St. Jude Mission. The ethicist will also contribute to the Section on Bioethics’ program development and research agendas.
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Scientific: Develop and implement scientific strategies for the production and usage of data across different scientific domains including bioinformatics, computational biology, cell-imaging, and cell-modeling Design multi-modal and dimensional data models which address a wide range of user needs, including Tempus-researchers and biopharma partners Create user documentation and best practices on data model usage for researchers, publications, algorithm development, and clinical workflow.
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The Tulane University Center for Brain Health (TUCBH) in the Center for Sport at Tulane University is a clinical care and research center for Traumatic Brain Injury (TBI), Physiological conditions, and Behavioral Health (BH) conditions such as post-traumatic stress, depression and anxiety.
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The Potency Group within Cell Therapy Analytical Development is responsible for potency assay development and functional characterization for cell therapy products. The Associate Scientist will assist in developing state-of-the art potency assays that support the company portfolio of preclinical and clinical-stage cell therapies.
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Provides oversight of case processing activities for the Xenon clinical development program and serves as safety data management subject matter expert (SME) on regulations and best practices for conventions and handling of safety data in Xenon’s global safety database (GSDB.
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The Research and Development Engineer works within the Applied Research Laboratory (ARL) and falls under the specific approved promotion guidelines. The ASR includes crime statistics and institutional policies concerning campus security, such as those concerning alcohol and drug use, crime prevention, the reporting of crimes, sexual assault, and other matters.
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We research, develop, and commercialize innovative digital health products and solutions by bringing together the full capabilities of our team, including product strategy and management, clinical expertise, partnerships, UI/UX design, usability research, clinical research and validation, software development, AI / Gen AI, and regulatory.
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Accountable for all aspects of small and large molecule analytical development including supporting preclinical and clinical drug candidates and commercialization/launch of innovator and generic API products.
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Our Lab is focusing on the earlier phase of HIV and/or TB transmission, the host and pathogen interactions, the generation of specific immune responses and, the development of novel vaccines using the Nonhuman Primate Model.
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The successful candidate will support the research and early development of NGS-based methods to improve clinical diagnostic test access, quality and performance for patients with cancer.
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Identify emerging policy issues and oversee the development of policy positions and recommendations related to clinical research studies and drug development. Provide health policy content expertise and serve as a resource for ASCO's legislative and regulatory activities, with a focus on clinical research and pharmaceutical development policy and relevant federal agencies including but not limited to NIH, NCI and FDA.
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Experience in utilizing platforms including IncuCyte, JESS, Flow based cell sorter, ELISA, and MSD in the context of oncology-based drug discovery is a plus. Design and conduct essential mechanistic experiments in cell biology, cellular biochemistry, molecular biology, and assay development.
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clinical research drug development jobs Company: 5py Us Quintiles Inc in TX, Us
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