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, projections, and various projects. Key Responsibilities Provide oversight of the departmental income statements and fund accounts by ensuring accuracy, performing analysis, and developing presentation summaries
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research aligned with the lab’s focus areas. Design and execute experiments in molecular biology, virology, and dermatologic disease models. Design experiments, conduct experiments, analyze data, prepare
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. An active participation in teams designing research projects and clinical trials as well as in report writing and publications is expected. Key Responsibilities: Contribute to clinical trial and protocol
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for complex and varied research, financial, and analytical work related to grant review and management. The primary responsibilities of this position are to assist Principal Investigators (PIs) with
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to supporting Dr. Olds’s administrative needs. Key Responsibilities: Assist Dr. Olds with administrative tasks including management of his calendar, schedule, and workflow. Attend meetings with Dr. Olds, taking
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events. Participate in study-related travel and offsite clinic events as needed. This is a part-time (0.5 FTE) position that reports directly to the Project Manager. Work Location: Why Join Us: Onsite
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the Quality and Compliance Program Director, the DSMC Manager, the Cancer Center Learning and Development Manager, Assistant Director of Clinical Research, and Clinical Research Faculty leaders to create a
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to clinical practice or experiential learning in their area of expertise. Key Responsibilities: Lead the design and implementation of a modern PharmD curriculum that incorporates innovation, promotes
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of human disease, therapeutic interventions, clinical trials, or development of new technologies. Clinical Science Professionals may also assist with epidemiologic and behavioral studies and/or outcomes
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required for research projects Assist Team Leads, Supervisors and/or management with creation and implementation of processes and procedures and quality improvement initiatives Assist and train junior team