University of Kansas Medical Center Research Institute, Inc.


The University of Kansas Medical Center (KUMC) is a leading academic medical center that integrates education, research, and patient care. It comprises three schools: the School of Health Professions, the School of Medicine, and the School of Nursing, offering a wide range of degree programs and fostering interprofessional collaboration. KUMC is dedicated to advancing health sciences through innovative research and providing high-quality clinical care.

Industries

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University of Kansas Medical Center Research Institute, Inc.


Services

Office of Clinical Trials Administration

Institutional office providing portfolio management, study activation coordination, regulatory guidance, and quality assurance support for clinical research studies.

Research Contracts Office

Service that reviews and negotiates research-related contracts and subcontracts, including confidentiality agreements, industry-sponsored research contracts, material transfer agreements and data use agreements.

Sponsored Programs Administration (SPA)

Central office for administration of externally sponsored research projects providing proposal support, award setup, compliance assistance, post-award management, and award monitoring resources.

Financial Services for Research

Fiscal services including stewardship of research funds, clinical trial finance, budget negotiation and systems/data analysis to support accountable management of extramural funds.

Research Development Office

Pre-award support offering proposal management, connections to reviewers and consultants, scientific writing and biostatistics consultation, and coordination of ancillary research documents.

Research Systems Support

Directory and operational support for research IT systems and applications used by study teams, including electronic IRB and submission tools, electronic data capture platforms, clinical research information systems, participant payment services, policy libraries, and a central help/contact route for technical assistance.

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Expertise Areas

  • Clinical trial management and study activation
  • Human subjects protection and institutional IRB oversight
  • Electronic IRB and eCompliance submission workflows
  • IRB reliance and single-IRB coordination
  • Show More (10)

Key Technologies

  • Electronic IRB systems
  • Electronic data capture (EDC) and survey platforms
  • Clinical research information systems (CRIS)
  • De-identified clinical data repositories
  • Show More (6)

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