CHS IRB submissions are to be submitted electronically through OneAegis: https://chsresearch.oneaegis.com/
If you have any questions regarding, OneAgeis, please do not hesitate to contact the IRB office at [email protected]
For assistance with all aspects of obtaining IRB approval for your research, and for assistance in submitting your materials to the IRB, please email [email protected].
All UCSF Faculty, Fellows, Residents, Medical Students, and Key Research Personnel must complete mandatory training in the protection of human subjects in research through the Collaborative Institutional Training Initiative (CITI). Information regarding this UCSF requirement can be found at:
To complete the training, go to www.citiprogram.org
Create a login & password, then choose UCSF as the affiliated institution.
Please contact the IRB Office at [email protected] for any questions.
As UCSF staff, you are required to submit your study to IRIS. This can be found in MyAccess.
For assistance or questions, please contact:
Christine Mergillano, CCRP
Regulatory Specialist
Clinical Research Center
155 North Fresno Street
Fresno, CA 93701
[email protected]
Richard Ward, BS, CCRC
Regulatory Specialist
Clinical Research, Oncology Services
785 N. Medical Center Drive West
Clovis, CA. 93611
[email protected]
Jamie Ellison, MBA
Regulatory Specialist
Clinical Research, Oncology Services
785 N. Medical Center Drive West
Clovis, CA. 93611
[email protected]