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is a full-time work from home remote position responsible for maintaining data integrity of multiple assigned research studies of all phases involving human subjects. In this role you would be
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our Clinical Trial Office (CTO), you'll collaborate closely with COH investigators, overseeing a diverse range of research studies involving human subjects. As a PCRC, you'll not only lead your disease
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techniques such as transplantation, extraction of bone marrow cells, and antibody staining · Isolate Peripheral Blood/Bone marrow mononuclear cells (PBMC) from Human Acute Myeloid Leukemia (AML
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to departmental core services, emphasizing positive leadership and human resource development. Pre-Award Management: Provides pre-award support for grant, foundation, and protocol proposals, ensuring timely
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using transgenic and transplantation mouse models of lymphoproliferative diseases, primary cells from patients, humanized mice, gene editing, classical molecular, cell biology, and biochemistry, and
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. · Act independently to determine methods and procedures of new projects. Qualifications: · Bachelors degree in a scientific discipline or equivalent with a Masters degree preferred. · 2-5
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or institutional core laboratories. Individuals appointed as staff scientists will receive a one-year fixed-term contract. Your qualifications should include: A Ph.D with a minimum of three years of human T cells
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, shaping the future of medicine through cutting-edge research. Clinical Research Protections provides support to the Data and Safety Monitoring Committee (DSMC). Research Protocol Analysts oversee human
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County and Clinical Network on license facilities. The Pharmacy Director in the area of Investigational Drugs will oversee clinical, operational, financial, regulatory and human resources management of all
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, experience in sequencing or protein structural data analysis is highly preferred. · Previous experience in working with animal models of human cancers · Literature knowledge of one of the three