Frequently asked Questions
- I’m a PVAMU student interested in conducting my own research project do I need IRB approval before I can begin?
- Can I be listed as the Lead Researcher on the IRB Application?
- Should I submit a new IRB application, or be added to my Faculty Advisor’s protocol?
- Is IRB review necessary if my study involves anonymous surveys or interviews?
- How do I apply for IRB review?
- How long does it take to obtain IRB Approval/Registration?
- How will I be notified when my IRB application is approved?
- How long is my approval good for?
Yes. Students conducting human subjects’ research require IRB approval or registration before they can initiate their project. See Definition of Human Subjects Research for more information. Please consult with the Human Research Protections staff if you are unsure whether your project constitutes human subjects research.
No. PVAMU doctoral students can not be Lead Researchers/Investigators on human subjects’ protocols. Faculty Sponsorship is required for all research applications to include outside investigators that desire access to the university student population.
When a student’s research project consists of the collection and/or analysis of data that is part of the scope of an existing faculty member’s IRB approved research, the student can be added to the Faculty member’s protocol, rather than submitting as Lead Researcher on a new IRB Application.
Yes. An application for Exempt Registration is required if you plan to conduct anonymous survey or interview research.
- Faculty Sponsorship – Find a faculty advisor who will sponsor and guide you throughout research process.
- Formulate your research question and study design. If your study involves interviews, surveys, or questionnaires identify the standardized instruments that will be used. If a new measure will be used develop your survey or questionnaire instrument or interview protocol.
- Define your sample population and develop recruitment procedures. See: Subject Selection and Recruitment.
- Determine how you will obtain informed consent. See: Informed Consent Preparation.
- All study team members are required to successfully complete for credit the Human Research tutorial and HIPAA tutorial, if applicable, Even non-PVAMU investigators on PVAMU protocols are required to complete the tutorial(s). Applications may be withheld pending tutorial completion. You may verify that research team members have completed the required tutorial(s) by entering their name on this webpage: Verification of Tutorial Completion.
- Complete the IRB Application. See: Protocol Preparation Checklist. Also see the 10 Most Common Reasons why Protocols are Deferred by the IRB.
- Faculty Sponsor and Department Chair’s signatures are required on IRB applications for student research. Applications will be withheld until all required signatures are provided. Please note that if your Faculty Sponsor, or any member of the study team is the Department Chair/Director, the signature of the next highest level of administrative authority is required.
- Submit the appropriate number of copies to the Office of Research Administration. See: How to submit an IRB Protocol for additional guidance.
- Save a copy of your application packet for your records and back-up all files relating to your application on your computer, as you may be asked to submit revisions following the Initial Review.
- See: “I’ve submitted my IRB Application. Now what happens?” on this page for more information about the IRB review process.
Full Committee protocols are reviewed monthly. The turnaround time from submission to approval generally takes 4-8 weeks for full Committee protocols depending on the completeness of the submission including the required additional documents (e.g., informed consent/assent forms, recruitment materials, questionnaires) and whether other PVAMU Committees must first approve the research (e.g., IBC, IACUC). See: Human Subjects Application and Protocol Preparation Checklist.
An official IRB approval letter and all approved documentation will be sent by e-mail to the Lead Researcher within a week of IRB approval. If you are listed on a full Committee protocol, Research Protections posts the IRB decisions the day after the meeting date via an e-mail request. See: Results of Full Committee Meeting.
Most full Committee protocols are approved for one year from the date of approval (the IRB may grant a shorter approval period). Continuation of an approved protocol requires submission of the Continuing Protocol Application. A research protocol is registered for three years and requires a yearly update. Continuation of a protocol beyond three years requires submission of a new IRB Application.
Was this information helpful? Provide Feedback or report broken links.