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with data managers to help design, develop and test appropriate informatics tools to meet study data, participant and sample tracking needs Helps to develop standard operating procedures Compiles
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development of specific department programs. Responsibilities 1. Assists with program planning and implementation. 2. Compiles, sorts, and organizes data for entry into a database, distributes program
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on cancer related clinical trials to ensure compliance with study protocol, University, state and federal guidelines. Compile comprehensive reports for Principal Investigators, DSMC and other committees as
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. Create and maintain files, compile reports, and manage, store, and disseminate information, ensuring security and compliance of information. Remain knowledgeable about program policies and procedures
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to the contracting and sponsored project management process, including preparing and submitting reports, analyzing and preparing data of work performed, compile reports, and other tracking and reporting tasks as
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and diagnostic tests. Assists in routine clerical functions such as filing of medical information in patient’s records, locating and compiling department charts, obtaining medical records from other
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from participants Documenting activities and outcomes in appropriate databases Compiling reports summarizing study progress Running basic statistical analyses (e.g., descriptives) to characterize study
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administrative tasks, including managing the team email inbox, generating reports, and compiling data from the Learning Management System. Responsibilities also include transcription, data entry, organizing and
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and/or participates in the advising-related portion of new/transfer student and parent orientation sessions. 9. Assists with data compilation, statistical reports, and correspondence, depending
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and/or participates in the advising-related portion of new/transfer student and parent orientation sessions. 9. Assists with data compilation, statistical reports, and correspondence, depending