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Research

Collaborative Institutional Training Initiative Program (CITI Training)

NUNM researchers and affiliates are required to complete various CITI Program trainings depending on their roles and responsibilities.

CITI Registration Information

If you are new to CITI training:

  1. Go to the CITI website at https://citiprogram.org/
  2. Click the “Register” button in the upper right hand corner
  3. Search for “National University of Natural Medicine” in the institutional affiliation box
  4. Complete the registration, answering “what is your role in research” with the option that best fits your role

If you have previously completed CITI trainings with NUNM and want to add an additional training:

  1. Log into your account at https://citiprogram.org
  2. Under “Main Menu/My Courses”, click on “National University of Natural Medicine Courses”
  3. Scroll down to the section labeled “My Learner Tools for National University of Natural Medicine”
  4. Click on “Add a Course”
  5. Select the desired courses

If you have previously completed CITI trainings with another institution and want to add NUNM to your existing CITI account:

  1. Log in to your existing CITI account
  2. Under the main menu, look for the blue bar that says “Click here to affiliate with another institution”
  3. Search for “National University of Natural Medicine” in the institutional affiliation box
  4. Complete the registration, answering “what is your role in research” with the option that best fits your role

Training Requirements

Trainings are required every five years.

NUNM Investigators and Study Staff (excluding students)
These requirements apply to internal researchers and study staff who are NUNM employees.

  • Responsible Conduct of Research
  • Human Subjects Research (includes HIPAA)
  • OSHA Bloodborne Pathogens
  • Good Clinical Practice (FDA or ICH version; FDA is recommended)
  • Clinical Research Coordinator – recommended

Student Researchers and Affiliate Investigators
These requirements apply to NUNM student researchers, external investigators and collaborators who are not NUNM employees.

  • Responsible Conduct of Research
  • Human Subjects Research (includes HIPAA)
  • OSHA Bloodborne Pathogens
  • Good Clinical Practice (FDA or ICH version; FDA is recommended) – only required if working on an NIH funded study

IRB Members

  • Responsible Conduct of Research
  • Human Subjects Research (includes HIPAA)
  • IRB Administration

If you have any questions please contact NUNM IRB Liaison, Emily Stack.