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UCI Clinical Research Coordinator Certification Preperation Series

UC Irvine Institute for Clinical and Translational Science is proud to present UC Irvine’s Clinical Research Certification Preparation Series, designed to prepare clinical research professionals for certification by the Society of Clinical Research Administrators.

Topics include:

  • Ethical Principles, Informed Consent, Safety
  • IRB Roles, Responsibilities
  • Clinical Trial Protocol and Amendments
  • Investigator Roles, Responsibilities
  • Sponsor Roles, Responsibilities
October 10, 2016: SESSION 1 »

Agenda

Speaker: Ruth Mulnard, DNSc, RN, FAAN

  • Introduction                                                  

  • Ethical Principles/ Informed Consent/Safety

Related Materials

October 24, 2016: SESSION 2  »

Agenda

Speaker: Laverne Estanol, MS, CCRP

  • Institutional Review Board (IRB/IEC)

  • Roles and Responsibilities                                                              

Speaker: Ruth Mulnard, DNSc, RN, FAAN

  • Clinical Trial Protocol / Amendments

Related Materials

November 7, 2016: SESSION 3 »

Agenda

Speaker: Beverly Algers, BSN, RN, CCRP

  • Investigator’s Roles and Responsibilities

Related Materials

November 21, 2016: SESSION 4  »

Agenda

Speaker: Beverly Algers, BSN, RN, CCRP

  • Investigator’s Roles and Responsibilities (con't)

Speaker: Lisa Jones, MS, CCRP

  • RedCap Database for Research

Related Materials

December 5, 2016: SESSION 5  »

Agenda

Speaker: Ruth Mulnard, DNSc, RN, FAAN

  • Sponsor Roles and Responsibilities

Related Materials

December 19, 2016: SESSION 6  »

Agenda

Speaker: Ruth Mulnard, DNSc, RN, FAAN

  • Sponsor Roles and Responsibilities (con't)

Related Materials

If you have any questions regarding this course please contact Diana Vigil; dvigil1@uci.edu; (949)824-1231.