151 data-"https:" "https:" "https:" "https:" "https:" positions at University of Kansas Medical Center
Sort by
Refine Your Search
-
regarding the status of tissue requests is required. Perform study-specific ECGs and transmit data to appropriate database as listed in the study protocol schedule of events. Reference and maintain a variety
-
. This position involves a range of technical duties, including conducting biochemical and other laboratory tests and experiments to gather data for research purposes. Responsibilities include performing
-
outcomes. Team Lesson Planning – Schedule and protect time for regular collaboration among the teaching team to review data, reflect on children’s progress and teaching practices, and plan for interaction
-
employer contribution and additional voluntary retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html Employee Type: Regular Time Type: Full time Rate Type
-
Principal Investigator. Job Description: Job Duties Research Overview: Design and conduct experiments and interpret data under the mentorship of the Principal Investigator (PI). Work independently and
-
, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https
-
Practice, Standard Operating Procedures (SOP’s), scope of practice and other state and local regulations as applicable. Ensure data collected for completed procedures is recorded on appropriate forms and
-
to designing and executing experiments and using various molecular (e.g., qPCR) and histological (e.g., immunohistochemistry, immunofluorescence) techniques to generate data. Interpret experimental results and
-
retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html Employee Type: Regular Time
-
the collection, compilation, documentation, and analysis of clinical research data. Monitors participants' progress including documenting and reporting adverse events. Participates in periodic quality assurance