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-center research study and/or multiple research studies. Compilate, register and submit study data. Monitor project databases and maintain a system of effective data flow associated with research protocol
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through cutting-edge research. Exciting opportunity for a detail-oriented individual! Join us as a Clinical Research Assistant I in which you will manage an assigned set of multiple research protocols
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proposals (e.g., R01s), ensuring scientific clarity, technical accuracy, and alignment with funding agency requirements. Collaborate with faculty to design and prepare new research projects for funding
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. 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 Associate Clinical
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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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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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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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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 attend clinic as
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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