Clinical Coordinator Trainings

ICTS Clinical Research Coordinator Professional Development

The Clinical Research Coordinator (CRC) Professional Development Series is an opportunity for clinical coordinators to come together, network with peers, and learn skills and opportunities to expand their professional growth and development.

The ICTS will be offering CRC Professional Development Series presentations, talks, and/or lectures on a quarterly basis. An email update will be sent out to the CRC Hubs on campus. If you would like to join the email listserv for these events, please contact Brooke Piercy.

Upcoming Sessions

More information coming soon.

If you have not already participated, please take a moment and click here to take a short survey. We would like to gauge your interest in which topics would be of greatest interest for upcoming sessions.

For more information, please contact Brooke Piercy.

Clinical Research Coordinator Training Program

The UCI Alpha Clinic offers the AC Clinical Research Coordinator Training Program (CRCTP) to support the workforce development in clinical research by introducing the job duties and responsibilities of a Clinical Research Coordinator and all training to become a certified CRC. Upon completion of the program, each trainee will have received training and in-depth knowledge of cell and gene therapy research and clinical trials for those interested in pursuing or continuing a clinical research career at UCI. This program is available for UCI undergraduate students who intend to pursue a career pathway as a clinical coordinator. This 10-week summer program totals to 100 hours of instruction and runs from June – August each year, weekdays from 9am -12pm. For additional information, please visit the AC CRCTP website.

For questions regarding clinical trial management or becoming a clinical research coordinator at UCI, please contact the Center for Clinical Research.

Past Clinical Research Coordinator Training Sessions

November 1, 2024
Presenters: Isela Hernandez, MS & Brooke Piercy, MA
February 2, 2021
Submitting to WCG IRB using the new WCG IRB Connexus
June 30, 2020
Training in CIRBI for Advarra: Managing an approved study, including writing amendments, continuing review, prompt reporting and closures
June 29, 2020
Training in CIRBI for Advarra: The reliance process and submission to Advarra for an initial review submission
June 25, 2020
Training in WCG-Western IRB (WIRB): Managing an approved study, including writing amendments, continuing review, prompt reporting and closures
June 23, 2020
Training in WCG-Western IRB (WIRB): The reliance process and submission for WIRB for an initial review submission
September 19, 2019
Research Revenue Integrity Experimental Tissue Resource (ETR)
May 7, 2019
Introduction to Clinical Trials Enterprise (now known as CCR)
January 29, 2019
Using Epic for Research
September 10, 2018
Starting a New Clinical Trial – Research Support Services
May 14, 2018
Pathways to Certification
December 14, 2017
CRC Networking Event
September 19, 2017
ACRP Online Training Consent 2 Contact; What is it and how can it help with recruitment USC Regulatory Boot Camp
May 16, 2017
Billing for Research Grants; Budgeting for UCIMC Services Research Budgeting; Federal Funding Clinical Trials – Industry Sponsored Budgets
March 21, 2017
Conflict of Interest Update Translation Services
January 2017
HIPPA Training
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