441 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "ETH Zürich" positions at Tulane University
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holiday working hours Good communications and personal relations skills Computer literacy Ability to use of two-way radios Required Education and/or Experience No prior experience or training required
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patient care for clinical trials subjects. The Research Nurse II assists with independent data and source documentation, adverse event reporting and maintenance of complete regulatory files, under direct
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and meet deadlines • Proficient computer skills, including word processing, spreadsheets, and social media • Availability to work a flexible work schedule, including nights and weekends • Travel with
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and alumni engagement. This role leads strategic planning, data and CRM operations, financial oversight, personnel administration, and communications and stewardship strategy and plays a key role in
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employer events, collecting and organizing data to support CMC programs, and supporting general career team operations. The ideal candidate will be a strong communicator, organized and detail-oriented, tech
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departments, gathering data and generating regular reports on program usage to be used for program evaluation; and perform other duties as assigned. Required Knowledge, Skills, and Abilities • Strong
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with a variety of community-based organizations preferred • Maintain data and files for participants own records, as well as program reporting • Enroll subjects according to protocol • Ability to acquire
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, both for animal and laboratory space. • Experience with non-human primate experiment and rodent handling Compensation Information This position is classified as "exempt, salaried" and is assigned to pay
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as required on lab equipment. Required Knowledge, Skills, and Abilities Knowledge of computers and laboratory computer software. Ability to accept direction and communicate effectively. Physical
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, and effective monitoring of clinical trial subjects. The Clinical Research Coordinator II is also responsible for all data and source documentation, adverse event reporting and maintenance of complete