152 data "https:" "https:" "https:" "https:" positions at University of Kansas Medical Center
Sort by
Refine Your Search
-
Listed
-
Category
-
Program
-
Field
-
RA will work on a number of projects in the lab as needs arise. For more information about the laboratory, please see our website (https://www.kumc.edu/school-of-medicine/academics/departments
-
. 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
-
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
-
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
-
. Tasks include retrieving and summarizing data and information from literature searches and research studies; assisting faculty with the preparation of grants, manuscripts, and all other scientific
-
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: Hourly
-
to the collection, documentation, and analysis of clinical research data. Additionally, the Clinical Research Coordinator monitors participant progress, documents and reports adverse events, and participates in
-
mammalian development while working collaboratively with faculty, investigators, and research staff to maintain high standards of scientific rigor, protocol adherence, and data quality. Job Description: Job
-
the Department of Pathology will contribute to ongoing research by performing experiments, collecting and analyzing data, and assisting with the preparation of reports and publications. This position provides
-
monitoring (RBM) or source data verification (SDV) monitoring. Ensure the protection of clinical trial participants by reviewing and verifying the informed consent process, subject eligibility and enrollment