840 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "Newcastle University" positions at University of Colorado in United States
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with and oversee the day to day operations of clinical trials and studies Obtain study subject’s medical history and current medication information, reviews research protocol inclusion/exclusion criteria
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while working with sensitive information. Ability to actively listen and share relevant information, anticipate problems, and provide solutions. Ability to prioritize multiple projects and tasks with
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for budgeting and financial data analysis in collaboration with the Director of Finance and Administration (DFA) and Associate Director of Finance and Administration (ADFA) including oversight of the department’s
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for the overall organization and implementation of assigned study protocols/clinical trials, including study start-up, subject recruitment, screening, consenting, and coordination of study procedures and data
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admission files from faculty review to program acceptance. Student Progression: · Compile and manage all student data for tracking, advisement, intervention, and resolution of academic issues related
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tasks and deliverables to maintain deadlines. Strong computer skills with Microsoft Excel and appropriate project management software. Ability to performs work professionally and produce quality work
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, complete, and process logs, documents, databases, and related materials and information. Provide support by researching issues and developing recommendations to resolve process, unit, and related issues
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generally, the role will also include supporting preparatory activities such as IRB and protocol preparation and submission; development of operating procedures and data collection tools; and contributing
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financial planning and analysis, human resources, data, and technology. This role fosters trust-based collaboration across academic, clinical, educational, and administrative domains. The role partners with
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a program solicitation; Project management; Maintaining and tracking regulatory data; Electronic Trial Master File systems and processes; Quality checks on published regulatory documentation; Content