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right fit for you! As a successful candidate, you will: Conduct protocol management for an assigned set of multiple research protocols. Maintain current and accurate protocol documentation; notify
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, shaping the future of medicine through cutting-edge research. We’re seeking a detail-oriented Clinical Research Assistant I to support the management of multiple research protocols, ensuring regulatory
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. Preferred qualifications: Solid knowledge of molecular biology is strongly preferred. 5+ years of research/laboratory experience. 2+ years of genomics assay and genomic instrument operation experience
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. The candidate requires a strong understanding of clinical trial planning, management and metrics is essential as well as the ability to focus on multiple deliverables and protocols simultaneously. S/he
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the unique issues that older adults with cancer face, and supportive care research. You will manage multiple research protocols to assure efficiency and regulatory compliance of the protocols. You will also
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, FOLFOX-3B—all of which completed with numerous biomarker-driven projects pending). Participate in paper writing of multiple research projects. Data sets will be electronic. No biological samples will be
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need them today. Reporting to the Supervisor of Clinical Research Division at City of Hope Duarte Medical Center, we offer multiple full-time on-site positions within the Clinical Trial Office (CTO). As
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today. Reporting to the Supervisor of Clinical Research Division at City of Hope Duarte Medical Center, we offer multiple full-time on-site positions within the Clinical Trial Office (CTO). As an
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on identifying methods to mitigate toxicities from cancer treatment, with the goal of improving long-term patient outcomes. As a successful candidate, you will: · Conduct protocol management of multiple
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therapeutics or nucleic-acid chemistry o Nanoparticle / liposome formulation and characterization o HTS assay development and robotic screening o Recombinant protein expression in multiple hosts o