112 data-"https:" "https:" "https:" "https:" "https:" "https:" uni jobs at University of Kansas Medical Center
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. This position needs to possess basic computer skills, be able to follow written and verbal instructions, learn and apply new standard operating procedures and policies. Job Description: Key Roles and
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to facilitate all aspects of study conduct, including subject recruitment, informed consent, data collection, and reporting. Job Description: Job Duties Study Coordination & Management: Coordinate multiple
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assessment reports) under the supervision of the Principal Investigator. Responsibilities include drafting protocols, screening and appraising studies, extracting and analyzing data, and preparing results
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outreach, participant recruitment, qualitative/quantitative data collection, scheduling, clerical duties, data management, purchasing, event planning, website content management and organizational tasks. May
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Department: SOM KC Cancer Center Clinical Trials ----- Clinical Trials Data Management Position Title: Clinical Data Coordinator Job Family Group: Professional Staff Job Description Summary
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of faculty investigators, this position plays a key role in recruiting and educating participants, ensuring accurate data collection, and maintaining compliance with regulatory and institutional standards
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information systems, new technical solutions, or process improvements. The BA must be broadly knowledgeable in the functionality of KUMC enterprise systems as well as KUMC business processes. The BA works
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, study procedures, data collection, and monitoring of participant safety while contributing to the overall quality and integrity of research operations. Job Description: Job Duties: Recruit, evaluate, and
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syllabus, case summaries and proctors exams Correlates grades and other activities associated with the clerkship Assists with submitting final grade to ASA Collects data and reports the student evaluations
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, and analysis of clinical research data. Monitor participants’ progress including documenting and reporting adverse events. Participate in periodic quality assurance audits of protocols. Job