- Education Opportunities
- In-service Education Training
- Past Classes and Slides
- Other Education Resources
Education Opportunities
UCSF Clinical Research Resource HUB's Suggested Training for Clinical Research: The HUB has published a useful checklist for both onboarding and ongoing training for Clinical Research Coordinators, PIs, and other research support staff at UCSF.
iRIS Interactive Tutorials: Visit iRIS Help website (MyAccess login required) for a suite of interactive online tutorials for working in iRIS.
In-service Education Training
Need an in-service for your department? In-Services are a great way to educate a team or department for specific topics and assure all attendees hear the same information. To request an in-service training session please fill out this form.
Questions? We encourage you to submit your questions to us using the "Ask Andy" Analyst of the Day form.
Past Classes and Slides
| Preparing a New IRB Application (currently unavailable) | Preparing Consent and Assent Forms and the Consent Process |
| Submitting Modifications and Continuing Reviews | IRB Introductory Training Archived Webinar (please register to view) or Slides (currently unavailable) |
| Post-Approval Event Reporting and Overview of UCSF's Subject Injury Program | Findings From Routine Site Visits Conducted by the Quality Improvement Unit (QIU) |
| Recruitment: Ethics, Regulations and Practical Solutions and Technology and Best Practices for Recruitment |
Note: The IRB was formerly known as the Committee on Human Research (CHR), which is the term used in some of these presentations.
Other Education Resources
UCSF
- Suggested Training for Clinical Research: The UCSF Clinical Research Training document provides essential and supplementary training resources for Clinical Research Coordinators (CRCs), covering areas like HIPAA, informed consent, Good Clinical Practice, and data security. Each training component includes links, requirements, and estimated completion times.
- Clinical Trials Operations (CTO):The Clinical Trials Operations (CTO) Unit serves as an institutional representative and advocate for the UCSF clinical trials community. The CTO aims to identify, assess and prioritize barriers for inclusive and efficient trials, and steward solutions to challenges that adversely impact clinical trials operations. View upcoming and past events.
- Responsible Conduct of Research: A guide for RCR training for UCSF learners and researchers at all levels — graduate students, postdocs, and faculty — and a resource for NIH training grant faculty and administrators.
- UCSF Clinical Research Resource HUB: Training
- Clinical and Translational Science Institute (CTSI)
Other Groups or Institutions
- Center Watch Resources
- University of Michigan Online Course: Valid Consent/Refusal to Participate in Research
Federal Government