350 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "UCL" "UCL" "UCL" positions at Tulane University in United States
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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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. 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
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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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. • Ability to organize and analyze activities, create and manage data, think strategically, and manage multiple projects effectively. • Ability to manage time effectively and meet deadlines. • Proficient with
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maintaining knowledge base relative to billing functions, internal and external regulations and documentation issues. This person must be able to work independently and process large quantities of data
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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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-service oriented office setting. Preferred Qualifications • Some college education. • Familiarity with a multi-line phone system, computer data entry, and word processing. • Familiarity with Microsoft
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health behaviors. • Assist participants with navigation of the health care system and processes. • Facilitate referrals for appropriate health information and services as recommended by the provider and
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experiments on field samples via laboratory analysis, including integration of data into a Geographic Information System (GIS), MRPP statistics and production of graphics. The medical research specialist must
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visits, data collection and entry, and quality control activities according to study protocol independently. The Clinical Research Coordinator II is also able to perform procedures required by the study