I’m a PVAMU student interested in conducting my own research project do I need IRB approval before I can begin?
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.
Can I be listed as the Lead Researcher on the IRB Application?
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.
Should I submit a new IRB application, or be added to my Faculty Advisor’s protocol?
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.
Is IRB review necessary if my study involves anonymous surveys or interviews?
Yes. An application for Exempt Registration is required if you plan to conduct anonymous survey or interview research.
How do I apply for IRB review?
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.
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.
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.
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.
How long does it take to obtain IRB Approval/Registration?
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.
How will I be notified when my IRB application is approved?
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.
How long is my approval good for?
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.
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