389 data-"https:" "https:" "https:" "https:" "https:" "https:" "P" positions at Tulane University
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Abilities Proficient in data collection and entry, tabulation and CRF formatting Excellent written, verbal communication, interpersonal and organizational skills Team player, dependable, focused and takes
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the principal investigator, field coordinator, and project manager to recruit participants from the Bogalusa, Franklinton, and Covington area WIC clinics. Responsibilities include data collection and implementing
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to manage multiple responsibilities in outpatient settings • Knowledge of computer programs for clinical data entry • Self-motivated with good organizational skills • Ability to work with a diverse population
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will support the Director of Annual Giving and the Executive Director, Health Systems. Primary responsibilities include budget tracking and processing; communications coordination; data and project
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Motor Vehicle Policy criteria to become authorized as a driver • Ability to lift up to 30 lbs. • Must be capable of sitting and standing in one location for long periods of time. • Basic computer
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Position functions to serve as OISS’ first point of contact and primary information resource representative for email, phone and walk-in inquiries. This position checks messages on office voicemail and
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at the full accountant level to include the maintenance, analysis, interpretation and reporting of financial accounting data and the application of generally accepted accounting principles and theories in
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, and Abilities • Administrative and management experience • Financial and budgetary development and management experience • Supervisory experience • Excellent computer skills including use of Excel and
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Relations, Corporate and Foundation Relations, Information Services and other departments throughout the University, fostering a culture of strategic coordination to maximize philanthropic impact and long
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. The Research Nurse I provides direct patient care for clinical trials subjects. The Research Nurse collects data and source documentation, adverse event reporting and maintenance of complete regulatory files