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. · Work with investigators to assure the clarity and accuracy of data presentations. You will advise and assist with creation of clear, appealing data figures, model overview figures, graphical abstracts
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protocols, while maintaining high standards of scientific rigor. Accurately record, analyze, and validate experimental data; generate figures and summaries to support ongoing projects and publications
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involves coordinating First in Human to Phase III and Investigator-Initiated Trials. Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory
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include experimental design, data interpretation, manuscript preparation, and supervision of lab operations, with collaboration across clinical and research teams to advance studies with direct diagnostic
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attending clinics as needed. You'll handle data compilation, registration, and submission, and maintain an effective system for data flow. Benefit from mentorship by experienced staff in a dynamic research
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research protocols to assure efficiency and regulatory compliance of the protocol, attending clinic as needed. You will be responsible for compilation, registration and submission of data; monitoring study
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; and managing inventory and supply lists.Additional duties include assisting with specimen or data collection for research projects or demonstrations; cleaning and maintaining glassware and laboratory
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store blood samples following study and safety guidelines. Utilize EPIC and various sponsor web portals for study documentation and data entry. Perform other duties as assigned to support research
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computational methods for cancer pangenomics using long-read sequencing data. Through TGen's Collaborative Sequencing Center (CSC), we have access to in-house PacBio Revio and Oxford Nanopore PromethION platforms
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candidate, you will: · You must have experience with flow cytometry, molecular biology techniques, cell culture, microscopy, tissue processing, immunohistochemistry, immunofluorescence, data analysis