Clinical Research Office
The Creighton University Clinical Research Office is your resource for all your clinical research needs. The office supports all learner and faculty initiated research in Health Sciences and School of Medicine from start to finish. We will guide you through the writing and statistical process, complete the IRB submission, work step by step through the initiation process and provide study management and record keeping. Read below for more information on how we can help with your study.
Types of Support:
- Investigator initiated study services for Creighton and CHI employed investigators (unfunded)
- National database studies
- Retrospective medical record review
- Prospective clinical trials
- Internal/external grants for Creighton and CHI employed investigators (LB595/LB692/NIH/Foundations)
- Industry Sponsored Trials for Creighton employed investigators
- Quality Improvement Projects
How We Help You Through Each Step of the Research Process:
Start Up
- Review and editing of protocol
- Consent creation
- IRB submissions
- Study pathway formation
- Study Proposal Form
Financial Services
- Budget
- Invoices
- Cost tracking
- Payment reconciliation
- Time/travel payment
Study Management
- Study coordinator
- Informed consents
- Study visits
- Record retention
- Study storage
Grant Preparation & Assistance
- Budget
- Statistics/analysis
- Bio-sketches
- Submission
Poster, Abstract and Manuscript Support
- University approved poster and presentation template
- Review and Editing
- Poster printing assistance
View complete description of research steps in the Clinical Research Pathway.
