311 master-"https:" "https:" "https:" "https:" "UCL" positions at Stanford University
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studies. Work under supervision of the principal investigator and/or study coordinator/supervisor. Duties include: Schedule and/or call subjects for appointments; contact participants with reminders
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; or Master's degree in a related scientific field. KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED): Comprehensive understanding of scientific principles. General computer skills and ability to quickly learn
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This position has been deemed critical by the Stanford Doerr School of Sustainability Dean's Office and is exempt from the hiring pause. This position is based on Stanford's main campus with consideration given
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Principal Investigators, Clinical Research Nurse Managers, Associates, and other stakeholders—to support patients with heart failure. Responsibilities include entering patient information into the electronic
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. Work under close direction of the principal investigator and/or study coordinator/supervisor. Duties include: Serve as primary contact with research participants, sponsors, and regulatory agencies
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assigned facilities in which they reside and focus, they work within a select team, participate in regular cross training, and provide back-up coverage for each other. The Building Manager will have primary
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questionnaires. Perform clerical duties in the preparation of regulatory documents. Maintain all forms and documents, including consent forms and master subject logs. File all appropriate correspondence. Assist
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consent forms and master subject logs. File all appropriate correspondence. Assist in the preparation and publication of research abstracts and manuscripts by working with biostatisticians, residents, and
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Coordinator who will be assigned to multiple clinical trial under the direction of the Principal Investigator and will work closely with the Amyloid Center Research Team. The clinical trials
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consent forms and master subject logs. File all appropriate correspondence. Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform