A.) Discuss the potential for GCRC support.
Take a few minutes to talk with us about your study. We have a wide variety of services to offer and we are familiar with potential pitfalls. A few minutes of work before submitting the application can save time once the study is under way.
B.) Ensure that your study meets the minimum requirements
- The study must involve human subjects
- The research must be NIH or investigator initiated
- A UNM physician must be part of the research team
- The study must have UNM HSC Human Research Review Committee approval
C.) Meet with the GCRC Biostatistician
Our biostatistician will help you with experimental design, data collection issues, randomization procedures, sample size/statistical power calculation, and data analysis.
D.) Meet with the GCRC Research Subject Advocate to develop an appropriate Data Safety and Monitoring Plan (DSMP)
E.) Check out our overview of the GCRC Application Process (Word format)