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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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deciphering their underlying molecular mechanisms in normal developmental processes and tumorigenesis. We cover research areas with relevance to RNA Biology, Cancer Biology, Chromatin Regulation, Cancer
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of various aspects of processing specimens, paying particular attention to safety practices. Work with physician or nurse to see that protocol related tests and evaluations are ordered per protocol guidelines
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of various aspects of processing specimens, paying particular attention to safety practices. Work with physician or nurse to see that protocol related tests and evaluations are ordered per protocol guidelines
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, processes, and forms to enhance the efficiency and the quality of work. Lead the preparation for external audits in collaboration with Research Quality Monitoring. Assist in the review of audited protocols
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. · Drive the continuous improvement of Quality systems, by establishing more efficient/effective processes and incorporating forward-looking technologies (e.g. electronic QMS, eBRs, AI-based approaches, etc
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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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the laboratory discoveries into the development and application of effective novel therapeutic strategies to treat cancers in the clinic. For more information about Dr. Chen’s lab, please visit here. As a
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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