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professional or personal experience. Good computer and organization skills. Strong time management skills and the ability to work independently. Special Instructions Summary Additional Information The University
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on the basis of sex in the education program or activity that it operates, as required by Title IX and 34 CFR part 106. The requirement not to discriminate in education programs or activities extends
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, pregnancy-related conditions, genetic information, or protected veteran’s status. The University does not discriminate on the basis of sex in the education program or activity that it operates, as required by
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conditions, genetic information, or protected veteran’s status. The University does not discriminate on the basis of sex in the education program or activity that it operates, as required by Title IX and 34
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conditions, genetic information, or protected veteran’s status. The University does not discriminate on the basis of sex in the education program or activity that it operates, as required by Title IX and 34
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. The University does not discriminate on the basis of sex in the education program or activity that it operates, as required by Title IX and 34 CFR part 106. The requirement not to discriminate in education
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laboratory activities and operations responsible for cost control, waste reduction, quality, and safety. Ensure test methodologies provide quality of results required and are in full compliance with regulatory
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safety during trial. 2. Proposes and negotiates alternatives for protocol. Educates staff about the scientific aspects of the study. 3. Applies pharmacological knowledge to help PI determine idiosyncrasies
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Spanish Responsibilities Clinical Research Coordinator (Non-R.N.) – Level 1 to 3 1. Oversee, assess and ensure participant safety and strict protocol implementation/adherence; oversee compliance with GCP