1,642 data-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"FCiências" positions at University of Michigan
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and compliance with IACUC, EHS, and any other regulatory bodies. Responsibilities* Supervise data collection and manage data for pre-clinical research projects related to bone healing Develop, design
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, throughout the course of employment. Learn more about the work modes . Additional Information We are committed to maintaining a safe and healthy work environment for everyone. As part of the onboarding process
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to the Golub Capital Nonprofit Board Fellows program, organize efforts around strategic initiatives and special projects, and manage multi-stakeholder data collection. You will collaborate with faculty, staff
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the reasons for your interest in this position and describe your particular skills and experience that directly relate to this position. Please submit contact information (phone and email) for 3-5 professional
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/Clinical Professor; however, the track and rank of the selected candidate will depend on qualifications. Additional Information Michigan Medicine, a leader in academic healthcare, invites visionary
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, flow cytometry, etc) Transgenic mouse procedures/surgeries General lab maintenance (ordering supplies, preparing stock solutions, dish washing, data organization, maintaining a lab notebook) Intellectual
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experience with medical data abstraction, working remotely with visually impaired participants, and a desire to gain expertise in both psychology and ophthalmology aspects of the project, in addition to a
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in the development of bargained for and student employees, in the preparation and presentation of food. Communicate with guests and respond to inquiries about the food; provide information about
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, consultations, preoperative evaluation, follow- up, plans of care Document all relevant data according to clinical and regulatory standards. Provide specialized education regarding disease-based and procedural
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trials to ensure compliance, data integrity, and safe study execution. Responsibilities* Protocol & Regulatory Expertise Serve as the primary expert on the IDE, IRB, and clinical trial protocol for all pre