Safety and Ethics are a very important part of research training. Most all research opportunities require initial training(s) to help protect yourself and others. It is the student's responsibility to ask their faculty mentor which trainings are required to participate in research. Below is a list of trainings offered to students planning on completing undergraduate research at Augusta University.
Note that ALL research that involves human or nonhuman animal subjects (even observations) must be approved or deemed "Exempt" by the Internal Review Board and/or the Institutional Animal Care and use Committee (IACUC). This includes all student theses. We provide many of the campus resources here below but the Research Office will have all the answers you need. It can be a little intimidating, so we strongly suggest that students naviage trainings under the mentorship of their research advisor rather than do so alone.
Please contact the appropriate training offices with your questions (linked below).
Students conducting resrearch with humans (live subjects, observations, surveys, etc) need to complete the Human Subjects Determination Request to see if they need to submit their research protocol to the IRB. The IRB Office provides group trainings and individual help as needed. Several helpful documents are:
First-time undergraduate researchers handling chemicals are required to attend an in-person training with the Chemical Safety Office. CURS hosts student-researcher orientated trainings once a semester, and additional trainings are held monthly with AU students, faculty, and staff.
Remaining trainings can be accessed online:
Trainings can be accessed online:
Students involved in research involving animals are required to abide by all federal, state, and institutional laws regarding ethical research involving live, wild, caged animals. Students should ask their advisor about all required training for thier particular project. Some relevant trainings are below.
Your PI must initiate the request BEFORE you submit any paperwork or attend trainings
CITI Training consists of different groups:
|Group 1: FDA Regulated Research||Investigational drugs, devices, and biologics. You must also complete the Good Clinical Practice module.|
|Group 2: Non-FDA Regulated Research||Prevention/intervention studies, community-based studies, investigator-initiated statues that do not involve the use of investigational drugs, devices, or biologics. You may be required to complete the Good Clinical Practice module.|
|Group 3: Human Derived Materials Research||Specimens, human tissue, genetic/reproductive material, medical records, databanks, and registeres. You may be required to complete the Good Clinical Practice module.|
|Group 7: Social and Behavioral Research||Surveys, questionnaires, interviews, photography, and tape recordings. You may be required to complete the Good Clinical Practice module.|
You can access these trainings online: