945 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "Univ" "UNIV" positions at University of Florida
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. Establish rapport with the patients to relieve anxiety. Schedule and coordinate patient appointments. Maintain daily records and patient charts. Collect patient data pertaining to clinical research. Expose
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in gathering valuable data for academic and business research, while you gain hands-on experience in the field of survey research. Conveniently located in downtown Gainesville at UF’s Innovation Square
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reservations after TA is established. Communicates information about travel and reimbursements, explains and answers questions regarding related matters within established guidelines, policies, and procedures
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clerical duties, i.e. appoints patients in computer, copies and files charts. Assists with other duties as required to maintain efficient flow of patient care. Helps the dental assistants with setting up and
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of clerical/customer service experience, preferably in a health care or education setting serving the pediatric population. One year of computer inputting data and reviewing patient demographic material
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information on benefits, please visit UFHR Benefits and Rewards (ufl.edu) Required Qualifications: Bachelor’s degree or an equivalent combination of education and experience. Preferred: Two years of experience
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and maintain pending purchase orders; follows up as needed Responsible for communicating status updates or information on purchases to requestors Lead the receipt and distribution of goods Lead the
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; or an equivalent combination of education and experience. Job Description: Coordination of Protocol Subjects & Data Collection Performs subject screening and consent for clinical protocols under direction
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the phone with diverse respondents. Your communication skills play a vital role in gathering valuable data for academic and business research, while you gain hands-on experience in the field of survey
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. Interpreting and collecting medical and clinical data for prospective and existing enrolled subjects on assigned clinical trials. Maintaining compliance with all internal and external regulatory and