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data collection and entry, and performs noninvasive cardiovascular tests according to study protocols. The Clinical Research Coordinator is also responsible for keeping all data and source documentation
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Coordinator assists the investigator team to develop study protocols and manuals of procedures. The Clinical Research Coordinator screens, enrolls and follows study participants, conducts data collection and
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assists the investigator team to develop study protocols and manuals of procedures. The Clinical Research Coordinator screens, enrolls and follows study participants, conducts data collection and entry, and
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intracellular cytokine staining, as well as analyze flow cytometry data using FlowJo. They will also be expected to develop new assays, optimize existing assays and SOPs, and train others on assays and SOPs
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. • Ability to prepare basic financial statements and reports; ability to accurately review and analyze financial information. • Ability to accurately enter financial data into appropriate ledgers, journals
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of data. The ability to communicate clearly and professionally with providers, administrators (DBON), and the TUMG staff. Responding timely and accurately to inquiries are key elements required
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responsible for front desk operations. The patient representative greats patients and visitors upon arrival, enters and verifies insurance information, answers phones, schedules appointments, checks out
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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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required occupational health screening, and any required drug screening will be conducted after a conditional employment offer has been extended. Compensation Information This position is classified as "non
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Summary Individual performs experiments in research laboratory to produce research data. Assist Principal Investigator with mouse breeding, experiments, assays and data collection. Perform dissections