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DESCRIPTION The Clinical Research Coordinator works under the direction of the Program Manager(s) and is responsible for day-to-day study activities including: participant screening and consent; study visits
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license may be requested in partnership with the School of Dentistry until the candidate is able to obtain a personal Minnesota dental license. Completion of a CODA approved advanced education program in
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, and stakeholder engagement. Job Responsibilities: Leadership: Lead the definition and refinement of product team work to ensure alignment with IAM program objectives, providing clear, actionable
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is carried out each year by full-time tenured and tenure track faculty members. However, as a professional and accredited program and professionally based discipline, we also rely heavily on part-time
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the facilitation of emergency use/compassionate use requests. These percentages are subject to change based on the needs of the role and program: Daily IRB Operations, IRB reviews, and IRB Panel
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program direction and ensure impact. Hire, develop, and supervise research project managers and administrative staff. Establish structure and operating practices that are fundamental to the success
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is carried out each year by full-time tenured and tenure track faculty members. However, as a professional and accredited program and professionally based discipline, we also rely heavily on part-time
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program activity viewable to all staff Report work activity on a regular basis using program forms, databases, or other formats as requested Help write, edit, design, review, and/or produce documents
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Qualifications: Strong written and verbal skills Experience with Canvas Preferred Qualifications: Knowledge and experience with the Certificate in Election Administration Program at the Humphrey School. Experience
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outages. Required Qualifications: Bachelorâ™s degree in computer science, cybersecurity, information technology, or a related field and 2 years of relevant experience, or Masters degree. Experience with