- HMS Community Values
- Introduction to Clinical Research Training
- Medical Education
- Clinical Scholars Research Training - United Kingdom
- Vanderbilt Hall
- Financial Aid
- Office of the Registrar
- Campus Planning and Facilities
- Ombuds Office
- Committee on Microbiological Safety
- Human Resources
- The Academy
- Office for Academic and Clinical Affairs
- Joint Committee on the Status of Women
- Global Health Research Core
- Global Clinical Scholars Research Training Program
- HMA Standing Committee on Animals
- Harvard Medical School Event Calendar
- Office of Diversity RIA Program
- The Dean's Perspective
- Department of Pathology
- Harvard Mahoney Neuroscience Institute
- OHRA Home
- Office of Research Subject Protection
- Cancer Biology & Therapeutics Program
- Celiac Program
- Department of Medicine
- HMS Information Technology
- IT News & Announcements
- Education Computing
- Federated Identity Services
- Information Security
- Student Computing
- IT Service Catalog
- Accounts & Access
- Administrative Applications
- Centralized End User Backup
- Computers & Software
- Email & Calendar
- Endpoint Services Program
- Mobile Computing
- Network & Wireless
- Storage & Servers
- Training & Consulting
- Web & Collaboration
- Research Computing
- Research Imaging Solutions
- Research Information Technology Solutions
- Research Storage Funding Model
- Safe Computing
- Get Help
- HMS IT User Privacy Statement
- HMS IT Careers
- HMS TransMed Program
- Introduction to Postgraduate American Medicine
- Office of Communications & External Relations
- Big Data In Healthcare
- Global Pediatrics Leadership Program
- Institutional Planning and Policy
- Master of Medical Sciences In Clinical Investigation
- Office of Global Education
- Portugal Clinical Scholars Research Training Program
- Safety Quality Informatics and Leadership
- South American Clinical Research Training Program | SACRT
- Southeast Asia Leadership Program
- Training to Teacher
- Shenzhen-HMS Initiative in International Education
- Contact @HMS
- Office of Global Education
- Human Resources
- Jobs @ HMS
- Dental Medicine
- Harvard University
- Contact us
For Student Researchers
First Year Scholars In Medicine Students!
Are you conducting a research project this summer? Do you need more information on the IRB or human subjects approval? Come check out our first year student IRB Workshops! Each workshop will be an introduction to IRB basics where you will learn what is required to submit for your summer project! You will also have the opportunity to discuss questions specific to your project with an IRB staff member. Join us for one of the sessions listed below to discuss your research.
Thursday, March 12 @3:45PM TMEC 324
Monday, March 16 @12:30PM TMEC 209
Wednesday, March 25@12:30PM TMEC 309
Wednesday, April 1 @3:45PMTMEC 126
Light refreshments will be served.
Frequently asked questions
1. Is there an instruction manual for submitting to the IRB?
2. Can a student serve as Principal Investigator (PI)?
Yes, students may serve as PI on “Not Human Subjects Research” and “Exemption” Requests. The Principal Investigator of these requests must be a Harvard LMA affiliate; however, a faculty appointment is not required. Any member of the faculty, staff, and/or student body may serve as PI for such protocols.
No, students may not serve as PI on non-exempt Human Subjects Research Applications (i.e., “Expedited” and “Full Board”). The Principal Investigator of such protocols must be a Harvard LMA faculty member. The IRB may make an exception to this policy on a case-by-case basis with appropriate justification (but customarily exceptions are not made for students).
3. How do I know which type of IRB review my project will require?
Most student projects do not meet the definition of research with “human subjects” or are eligible for an exemption determination (which must be made by the IRB). Some projects, however, depending on procedures and risk level, are reviewed on an expedited basis or require Full Board review. For help determining which type of review your project will require, call a member of the Quality Improvement Program (QIP) or your department-assigned IRB Review Specialist
4. How do I submit an IRB application?
The IRB submission process is conducted electronically, through ESTR: Electronic Submission, Tracking, & Reporting. One can log onto ESTR using their HUID and PIN. Click “Create New Study” and follow the system prompts; upload study materials as appropriate. The ESTR support website provides further instruction. For ESTR technical support, email email@example.com.
5. What IRB forms do I need to submit?
Harvard LMA IRB forms and instructions are available for download through Harvard’s electronic submission system, ESTR: Electronic Submission, Tracking, & Reporting. You will be prompted as to where they should be uploaded within the ESTR.
6. How long does IRB review take?
IRB review turnaround times may vary depending on the quality of the IRB submission. The below “target” turnaround times assume that the submission is complete and the Principal Investigator/Primary Contact is responsive. Applications requiring review by the convened IRB (“full board review”) should be submitted at least 45 days prior to a scheduled full board meeting. Click here for the list of the HMS and HSPH full board meeting and submission dates.
|Not Human Subjects Research Determination||1 week|
|Exemption Determination||1 week|
|Initial and Continuing Applications||2-3 weeks|
7. May I conduct international research?
Many Harvard LMA students do conduct international research. Ensure that you contact the host country contacts well in advance as their IRB review process may take longer than that at Harvard LMA. You may not begin your human research procedures (including recruitment) until all IRB approvals have been obtained.
8. If I have local IRB/another IRB’s approval, do I need Harvard Longwood Medical Area IRB approval?
When you are acting as an agent1 and conducting human research, Harvard is considered engaged and Harvard LMA IRB review is required. If, however, another institution is planning to conduct IRB review, it may be appropriate for HSPH/HMS/HSDM to cede IRB review to that institution.
9. What does “reliance on another institution” mean?
When multiple domestic institutions are engaged in the Human Research, a reliance agreement may be executed (i.e., cede review, or IRB Authorization Agreement) allowing an investigator to designate one institution as the Reviewing Institution (responsible for IRB review). Other engaged institutions would then rely on the Reviewing Institution’s IRB rather than conducting their own concurrent review. Reliance is not automatic, i.e., there is formal process and request form to put such an agreement in place. Click here for more information.
10. Who needs to complete human research training?
Researchers working directly with human subjects or data/specimens that he or she can link back to individual subjects must fulfill human research training requirements every three years. All Principal Investigators (PIs), Co-Investigators, and those meeting the NIH definition of “Key Personnel” must complete training regardless of whether or not they have access to identifiable data/specimens or contact with subjects.
Harvard’s online human research training curriculum is available through the University of Miami’s Collaborative Institutional Training Initiative (CITI) Program. Those who attend 3 QIP Education Sessions will receive Human Research training refresher credit. Click here for more information on human subjects training requirements.
11. Does the Harvard LMA IRB accept NIH training?
No, NIH training is not accepted. Harvard’s online human research training curriculum is available through the University of Miami’s Collaborative Institutional Training Initiative (CITI) Program. Click here for more information about CITI including how to access Harvard’s curriculum.
12. As long as I submit my application to the IRB, can I proceed with my research?
No, official IRB approval/determination must be received prior to conducting any human research activity (including recruitment or identifiable data analysis). A formal notification letter will be available in ESTR and emailed to the Principal Investigator and Primary Contact once IRB review is complete.
13. What is the deadline for PIM (Pursuing Inquiry in Medicine) projects/summer projects/etc.?
The deadline for PIM projects is April 15, 2014.
The IRB has no specific deadline for Non-PIM projects; however, IRB review and approval should be secured before implementing human research activities (including recruitment) in the field. Check with your advisor/department for additional deadlines.
14. How can I be added to the study team of an already IRB-approved project?
If you will be involved in participant interaction or intervention or have access to identifiable data you should be added to the project’s study team. For existing Harvard LMA IRB-approved studies, the PI will need to open a Modification in ESTR: Electronic Submission, Tracking, & Reporting selecting “Study team member information” where prompted.
For studies in which HSPH/HMS/HSDM is relying on another institution for IRB review please contact the Harvard LMA IRB Coordinator at firstname.lastname@example.org. When contacting the Coordinator, please provide a copy of the original protocol approval letter. Next steps will be determined once the Coordinator can review the other institution’s IRB approval.
15. What is meant by “coded” vs. “de-identified” data/specimens?
“Coded” refers to samples or data labeled with a code (e.g., a number), rather than a person’s name or other personal identifier. Such code can be traced or linked back to the sample donor/data provider by the person who retains the key, e.g., coding system/crosswalk. If such a key is in existence (whether or not the Harvard LMA investigator has access to it, the data/specimens are considered identifiable). To learn of ways in which coded data may become “de-identified,” contact a member of the Quality Improvement Program or your department-assigned IRB Review Specialist.
“De-identified/anonymized” refers to samples or data that may have identified human subjects at one time, but all identifiers or codes have since been removed and destroyed
16. My study materials, e.g., survey, interview, etc., are not yet developed. Can I submit these later for IRB review?
Where study materials have not yet been developed, note this in your application. If possible, provide draft copies of all study materials even if they may change later. Submit all finalized materials for review/approval via modification before use in the field. As a reminder, no research activities involving human subjects may occur without written approval from the IRB office. If study materials change during the course of your project, these materials must undergo IRB review and determination before implementation in the field.
17. Who can help me?
For questions about an anticipated submission, contact a member of the Quality Improvement Program (QIP) staff.
For ESTR technical questions, email email@example.com.
1 Agent: An individual who is an employee or student is considered an agent of Harvard School of Public Health, Harvard Medical School, and Harvard School of Dental Medicine for purposes of engagement in Human Research when that individual is on-duty in any capacity as an employee or student of HSPH. Specifically, it is an individual who, by agreement or otherwise, may act on behalf of the School and bind it by words or actions; a person who represents the School by its authority or delegated authority.
An individual who is not an employee is considered an agent of HSPH/HMS/HSDM for purposes of engagement in Human Research when that individual has been specifically authorized to conduct Human Research on behalf of HSPH/HMS/HSDM.
The Office of Human Research Administration (OHRA) will consult with the Office of the General Counsel (OGC) to determine whether someone is acting as an agent of HSPH/HMS/HSDM when it is unclear whether the individual meets this definition.