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issues identified by the RSC. Ensure information is provided to the investigator and requested changes are made per committee recommendations. Send approval documents to investigator. Function as Chair
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commitment to excellence and innovation. May participate in relevant committees, task force, or other similar activities. Maintain confidentiality of medical center, employee, and patient information. Handle
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, collection, compilation, documentation and analysis of clinical research data. The Clinical Research Coordinator will monitor participants’ progress including documenting and reporting adverse events and
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Problem solving Interpersonal skills Computer skills Required Documents Resume/CV Comprehensive Benefits Package: Coverage begins on day one for health, dental, and vision insurance and includes health
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. Perform research and interpretation of experimental results and analysis of data. Prepare manuscripts for publication in scientific journals based on experimental results. Participate in regular
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breast cancer research. This position will assist in entry level clinical research activities including collecting information from patients/study participants and ensuring study activities are performed
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Department: SOM KC Cancer Center Clinical Trials ----- Clinical Trials Data Management Position Title: Clinical Data Coordinator - Cancer Center Job Family Group: Professional Staff Job Description
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. https://www.kumc.edu/human-resources/benefits.html Employee Type: Regular Time Type: Full time Rate Type: Hourly Compensation Statement: The pay range listed for this position is determined by our
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data at the regional and national levels. Serve on hospital, university, and departmental committees as assigned. This job description is not designed to cover or contain a comprehensive listing of
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accountability, and data documentation. Recognize and report adverse events, deviations, and unanticipated problems in a timely manner to the Principal Investigator for review. Assist the Principal Investigator