117 data-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"L2CM" positions at City of Hope
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& Clinical Trials Gain real-world insight into: Disease modeling Translational research Clinical trial design and implementation How to write and structure a clinical trial Data analysis and scientific
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multi-site research. · Oversee data management systems for secure archiving, traceability, metadata capture, and reproducible quantitative analyses. · Manage scheduling, staffing
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current knowledge and requirements of relevant protocols. Performs extensive QC visits to confirm appropriate source documentation in electronic health record (laboratory data, transfusion services records
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basic science and translational projects in genetics, epigenetics, and precision oncology of gastrointestinal cancers. · Generate data for grant applications and prepare manuscripts
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with Principal Investigators (PIs) and their research staff including but not limited to clinical research coordinators, research nurses, monitors, data coordinators, as well as the various committee
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immunotherapies. As a successful candidate you will: · Performing experimental procedures · Manage data, analyze, and report findings · Write scientific papers · Work with PI and
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at the Arthur Riggs Diabetes Metabolism Research Institute of City of Hope. Built upon her interdisciplinary training in medicine, vascular biology, bioengineering, and data science, Dr. Chen leads
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regulatory requirements and the thorough collection, recording and maintenance of data and source documentation. The Clinical Study Coordinator collaborates with Investigators in review of subjects
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for the quality assurance/control management of OnCore study calendar specifications and financial console data entry (parameters, protocol related, subject related, and milestones) ensuring alignment with
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establish and maintain relationships with patients, visitors and other hospital personnel, while assuring confidentiality of patient information · Compile and submit data on appropriate forms