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regulatory compliance with the protocol. You will be responsible for compilation, registration and submission of data; monitor study compliance and maintain a system for effective data flow associated with
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. Her team is investigating biological processes that are critical to the progression of cancer and other diseases by using quantitative super-resolution microscopy. For more information on the Jovanovic
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responsible for abstracting and managing clinical, pathological, and outcomes data from electronic health records into research databases, ensuring accuracy and regulatory compliance throughout. This role also
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participants are appropriately registered and maintain documentation of participant registration. · Compile and submit data on appropriate forms according to protocol requirements. · Perform
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support external partnerships and revenue‑generating services. Informatics and Data Management Collaborate with Research Informatics and leadership to ensure accurate biospecimen data management within
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immunotherapies. Data from the group and others have demonstrated that the microbiome can be a potent modulator of treatment efficacy and toxicity. Using a multidisciplinary approach, including microbiome
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established protocols, while maintaining high standards of scientific rigor. Accurately record, analyze, and validate experimental data; generate figures and summaries to support ongoing projects and
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trial quality and regulatory compliance. This position works collaboratively with investigators, research staff, pharmacy, and leadership to identify compliance gaps through active data analysis using
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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
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research studies. Compilate, register and submit study data. Monitor project databases and maintain a system of effective data flow associated with research protocol(s). Facilitate and manage multi-faceted