225 data-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"I.E" positions at University of Vermont
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hospital or inpatient health care facility is recommended. Familiarity with clinical procedures is useful. Anticipated Pay Range $25 - $35/hr Other Information Ten month appointment will be from September 1
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Qualifications Experience with NIH grant management, staff management and training. Anticipated Pay Range $26.00 - $31.50our Other Information Special Conditions A probationary period may be required, Contingent
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requested. Accesses information utilizing desk top applications. Ensure training and safety programs are being followed. Provide general administrative support to manager. Schedule inspections of buildings
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communications with faculty, staff, and student participants. Anticipated Pay Range $60,000 - $70,000 Other Information Special Conditions A probationary period may be required, Contingent on continued funding
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process for overall student staff experience. Supervise the team of 20-25 student Information Desk Assistants for the Davis Center including hiring, training and supervision. Responsible for the overall
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information for at least three references. Please also include a separate statement addressing how you, as a faculty member, would enhance and advance the impact of Our Common Ground values at UVM and among
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statement of teaching interests and experience, evidence of teaching effectiveness, and contact information for at least three references. Please also include a separate statement addressing how you, as a
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pounds occasionally. Specific physical requirements may apply based on job functions. Effective communication, customer service, and computer skills required. Desirable Qualifications Certification as a
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, sponsor representatives, and laboratory staff. Support the preparation and management of study-specific and regulatory documents. Collect, maintain and report data from clinical research studies. Perform
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, sponsor representatives, and laboratory staff. Support the preparation and management of study-specific and regulatory documents. Collect, maintain and report data from clinical research studies. Perform