Nutrition guidelines for specific cancers 3. Clockwise from upper left: Jonathan Lu (Stanford), Karly Kampshire (UCSF), Raj Fadadu (UCSF), and Dr. Arianne Teherani (UCSF) host the education and curriculum reform session during the NorCal Symposium on Climate and Pandemic Resilience in Health Care on September 25, 2020. While this general list is a good starting place, we recommend that you speak to your Principal Investigator or supervisor to see which topics are most important. In particularly, new CRCs are strongly encouraged to sign up for CRC Bootcamp, which is focused on basic knowledge that is beneficial for … Welcome to Human Resources at UCSF and UCSF Health. It reviews the basic components of the CRC role at UCSF. Logistics. Accelerate is managed by the UCSF Clinical and Translational Science Institute (CTSI).Resources presented are offered by CTSI and other campus units. Please take a look at our Frequently Asked Questions: FAQs Study Best practice considerations when opening a new study to avoid management problems. Whether you're new to UCSF and need to learn the procurement system or an old-timer who needs some refresher courses, we have webinars and training guides as well as the latest system updates. Infection Control Training * Audience: 1. Please review the Suggested Training for Clinical Research checklist created for Clinical Research Coordinators (CRCs), PIs and other research support staff at UCSF, both for onboarding and ongoing training. Below are slides from past classes brought to you by the UCSF CTSI, HRPP and CRC Council: 490 Illinois Street, Floor 6, San Francisco, CA 94143, © 2013 The Regents of the University of California, Submitting COVID-19 Research to the IRB (New Studies & Modifications), Expanded Access – Individual Patient (SPIND), Enrolling subjects who are Legally Blind, Illiterate, Cannot Talk or Write, Post---Approval Reporting Requirements Summary Sheet, Reporting & Responding to Concerns & Complaints, UCSF IRB Clinical Research Tools, Checklists and Templates, Clinical Trial Coverage Analysis, Billing & Budget, The HUB: Suggested Training for Clinical Research Coordinators, HIPAA Training (required for all UCSF workforce members), NIH Clinical Research Training Resource for CRCs, Research Protocol Standard Operating Procedures Presentation, Guidance for an FDA Audit, Sponsor/CRO Monitoring Visit, and Other Resources Available on The HUB, Overview of Regulations That Drive Monitoring Visits and FDA Audits, What to Expect During an HRPP Quality Improvement Unit Routine Site Visit, Update on Monitoring & Electronic Medical Records at UCSF. Clinical Research Coordinator Council Yearlong Inquiry Program (YIP) - Provides support and training in clinical and translational research for medical, dental, nursing, and pharmacy students in a one-year fellowship. Suggested 2014 IPPCR courses for UCSF CRCs, Module 0 - Introduction: History of Clinical Research: A Merging of Diverse Cultures (Running time: 60 minutes), Module 1 - Study Design and Statistics: Unit 2 (Clinical Research from the Patient's Perspective, 30 minutes); Unit 4 (Overview of Clinical Study Design, 90 minutes) and Unit 6 (Design of Epidemiologic Studies, 90 minutes), Module 2 - Ethical, Legal, and Regulatory Considerations: Unit 1 (Ethical Principles in Clinical Research, 60 minutes), Module 3 - Preparing and Monitoring Clinical Studies: Unit 1 (Data and Safety Monitoring Committees, 90 minutes); Unit 6 (Evaluation of a Protocol Budget, 90 minutes); Unit 8 (Data Management & Case Report Form Development in Clinical Trials, 30 minutes); and Unit 10 (Data & Non-Data Aspects of Quality Control in Clinical Studies, 60 minutes). 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