The office is supportive in nature, facilitating research through the following processes (offered in a limited capacity before Spring 2008):
- Providing clinical research support to investigators
- Mentorship of new study investigators
- Protocol development
- Research development
- Assessment of study feasibility
- Project review and evaluation
- Study personnel requirement assessment
- Regulatory documentation assistance/direction
- Directions regarding required documentation
- Information on requirements for safety boards and safety reporting
- Study budget development
- Review of project for costs incurred by study vs. sponsor’s suggested funding
- Contract pre-review assistance
- Preliminary review for issues of conflict with MSU standard language requirements
- Assessment of funding mechanisms
- Advice for pursuit of funding sources
- Direction to other sources of university assistance
- Refer to departmental/other with needed area of expertise
- Serving as the contact point for potential sponsors; linking research opportunities with qualified investigators
- Ensuring research is conducted in compliance with up-to-date required regulatory and financial guidelines
- AAHRP requirements for contracts and consent forms
- Medicare research billing guidelines
- ClinicalTrials.gov registration
- Research data security issues