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. · Train new associates on GMP, including Good Documentation Practices, Aseptic Techniques, Gowning and Safety. Additionally, you will update training records and ensure adherence to the training program
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Manufacturing and analytical development for cellular immunotherapy products. This role involves performing QC assays, release tests, and assay development tasks, including cell viability, Flow Cytometry, ELISA
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modify protocols. Write standard operating procedures and reports. Maintain records of work performed, including results and methodology; utilizing records may calculate, graph, and compile data. Develop
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drug development, with strong potential for publication in high-impact journals. Our research aims to uncover fundamental mechanisms of leukemogenesis and solid tumor progression, with a particular
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Aging is led by Dr. William Dale and is housed within the Supportive Care Research and Training Division. Our research program focuses on studies related to cancer and aging, exploring the unique issues
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pioneering the development of neural stem cell (NSC) and extracellular vesicle (EV)-based therapies for neurodegenerative conditions, including traumatic brain injury (TBI), chemotherapy-related cognitive
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. · Perform comprehensive molecular validation and phenotyping techniques. · Support manuscript development, figure design, and integration of interim research findings to drive research progress. Your
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program and its educational offerings. You will serve as a project manager, navigating the regulatory review process for each of their research studies, ushering manuscripts thru the submission and revision
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Administrator generally works pacific time zone business hours. Position Summary: Coordinates and develops coverage analyses and budgets for both industry sponsored and non-industry sponsored clinical trials
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modify protocols. Write standard operating procedures and reports. Maintain records of work performed, including results and methodology; utilizing records may calculate, graph, and compile data. Develop