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pertinent clinical and protocol information on request forms. Develop and maintain knowledge of various aspects of processing specimens, with particular attention to safety practices. Identify and communicate
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with the QA Officer for preparedness for inspections by regulatory agencies so that there is a positive outcome and a minimum disruption in the daily operation and ensure that agency inspectors
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for identifying potentially eligible patients for each study. The CRN presents trial concepts and details to the research subjects, participates in the informed consent process, enrolls, and coordinates care
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, regulatory compliance, and study oversight. In this role, you will be responsible for attending clinics as needed, ensuring smooth data compilation, registration, and submission processes. You will monitor
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deep understanding of the entire reprogramming process, from the sourcing of somatic cells to the final characterization and banking of high-quality, pluripotent lines. This expertise involves mastering
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epitope selection pipelines. · Experience in molecular virology methods, and antigen presentation and processing as applied to human and murine oncology. · Ability to independently document
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Oncology, JNCI, Clinical Cancer Research, Nature Communications, Nature Reviews Gastroenterology and Hepatology, Annals of Surgery, etc. If you are passionate about some of the following things we
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reporting facilities. Trains and assists in orienting new statistical staff. Monitors project progress and maintains division records and files. Documents computer programs and electronic databases. Engages
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environment. As a successful candidate, you will: · Manages and maintains protocol documentation and regulatory documents for IRB, DSMB, and PRMC/CPRMC. · Compiles, submits, and processes data
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release processes concerning clinical trial supplies. Assist Biospecimen Coordinators by supplying collection materials for diverse research studies and ensure efficient distribution among hospital