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department standard operating procedures, under the supervision of the Principal Investigator (PI) and supervisor. The Clinical Research Data Specialist is responsible for the compilation, registration and
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is responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, adherence to SOPs, and all applicable regulations and guidelines. CORE JOB FUNCTIONS
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all proper documentation uploaded. Gather and compile necessary documentation for Business Office while ensuring compliance to UM policies and procedures. Assist with student expense reimbursements
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, and/or academic support units throughout the University. Coordinates the collection, compilation, and analysis of program activity data. Drafts comprehensive, statistical, and/or narrative program
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and procedures for program. Assure quality control and make recommendations for improvement of work methods and technology to increase productivity. Oversee the assembly, compilation, and processing
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. Coordinates the collection, compilation, and analysis of program activity data. Drafts comprehensive, statistical, and/or narrative program reports and evaluations, and monitors program effectiveness, making
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. Performs literature research. Compiles reference and statistical data into standard formats. Analyzes and presents data and information in written, oral or graphical forms. Documents experiment results and
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) position. The incumbent provides support in the performance of research related tasks for the assigned department(s) including data compilation, manipulation, and presentation. Additionally, the Research
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interpret accounting data. Ability to compile, organize, interpret, and communicate accounting data and results concisely. Ability to manage a budget and work within the constraints of that budget. Strong
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/ clinical tests with data collection schedules, established time-points; manages progress of study participants through protocol; expedites overall study progression. Coordinates the compilation