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to the Associate Director (AD). The COE's primary goal is to develop and lead the Cancer Center in facilitating catchment area community-engaged research and programs. This includes maintaining
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. As the Clinical Research Coordinator, your primary responsibility revolves around upholding the integrity of data across various research studies involving human subjects. This involves tasks such as
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in professional development activities and attends meetings as required. Your qualifications should include: • Master's in statistics, biostatistics, or related field • 3-5 years
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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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general supervision of the Principal Investigator, or designee, the RA II directs the work of a laboratory or undertakes research projects in collaboration with academic supervisor, making innovative
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and identity assays for release and characterization of these therapeutic products. · You will be expected to perform high quality original research work, participate in the clinical translation
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sponsors and COH departments to determine suitable coverage justifications and cost allocations for unique clinical trial procedures. As needed, works with Principal Investigators and study teams
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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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vitro models of the stromal niche, Dr. Danilov’s laboratory models lymphoid disease in vivo. Dr. Danilov’s research is highly translational and involves work with primary samples from patients with
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/research staff, Principal Investigators. Ensure quality assurance: of banked specimens. Adhere to regulations: regarding protected health information (PHI), IRB, and HIPAA. Maintain compliance: with City of