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to join our Clinical Trials Office team. As a Principal Clinical Research Coordinator (PCRC) you will be responsible for serving as a lead within you respective disease team mentoring new staff, providing
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to join our Clinical Trials Office team. As a Principal Clinical Research Coordinator (PCRC) you will be responsible for serving as a lead within you respective disease team mentoring new staff, providing
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, shaping the future of medicine through cutting-edge research. Under the direct supervision of the Principal Investigator, or designee, the Research Associate I performs a variety of routine and increasingly
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outcomes through two main research areas: Investigating the biological mechanisms underlying tumor progression: We use single-cell and bulk multiomic techniques to profile tumor samples, focusing
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, shaping the future of medicine through cutting-edge research. The Summer Academy Instructor will work under the supervision of Eugene and Ruth Roberts Summer Student Academy program grant Principal
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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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foundational entities to fund projects. Collaborate with internal and external research teams, laboratories, and pharmaceutical companies . Draft original research and review articles and publish in peer
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the department chair, one of the main goals is to foster translational and correlative studies to bridge basic science and clinical trials.
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advancements tailored to hematological malignancy patients. As a successful candidate you will: · Perform genotyping · Amplify plasmid · Procure reagents/supplies · Master mouse techniques such as
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, shaping the future of medicine through cutting-edge research. Under general supervision of the Principal Investigator, or designee, the Research Associate II (RAII) directs the work of a laboratory or