122 data-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"SciLifeLab"-"IFM" positions at City of Hope
Sort by
Refine Your Search
-
involves coordinating First in Human to Phase III and Investigator-Initiated Trials. Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory
-
; 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
-
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
-
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
-
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
-
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
-
candidate, you will: · You must have experience with flow cytometry, molecular biology techniques, cell culture, microscopy, tissue processing, immunohistochemistry, immunofluorescence, data analysis
-
performed, including results and methodology; utilizing records may calculate, graph, and compile data. Develop techniques and expertise in one or more areas relevant to laboratory research projects. Ensure
-
extensive review of case report forms and study data, utilizing medical records, laboratory data, transfusion services records, and any other source used to produce study data. Generates an audit report or
-
current and accurate protocol documentation; notify investigators of pertinent protocol changes. Maintain and complete regulatory documents for IRB, DSMB, and PRMC/CPRMC. Compile and submit data