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Committee on Clinical Investigations (CCI) submissions, together with the Principal Investigator of the study. Creates and prepares data collection statistical reports and analytical summaries
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. Analytical skills to gather and interpret data in which the information or problems are complex. The posted pay range is Boston Children's reasonable and good-faith expectation for this pay at the time of
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on submissions and track progress to review and approval. Creates and prepares data collection reports and analytical summaries for the research team, ensuring timely review and analysis. Responsibilities may
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laboratory activities in compliance with applicable regulations and protocols. Conducts literature searches and reviews, compiling information for journals and suggesting uses for new techniques to the P.I
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IRB documentation and submissions in conjunction with the Principal Investigator and/or other members of the research team. They will also conduct data collection activities and prepare analytical
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implementation, completing required forms and reporting results, and regulatory submissions. Conducts data collection activities and may prepare analytical reports on study results. Follows established clinical
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(training provided). Prior experience with IRB/regulatory processes. Experience with EPIC or other EMR systems. Comfort with basic statistics, data visualization, or analytic tools (e.g., R, Python, STATA
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, completing required forms and reporting results, and regulatory submissions. Conducts data collection activities and may prepare analytical reports on study results. Follows established clinical study
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laboratory, mostly by reviewing patients' charts and entering data in databases (likely for use on AI related projects). There will also be opportunities for participation in various efforts related
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); conducting a QC check of completed CRFs prior to submission for data entry; coordinating resolution of all data queries. Maintaining regulatory binders, case report forms, source documents, and other study