Login to access important UCSF HR content. Principles of Good Clinical Practice (GCP) Location Parnassus N-417 & 423 . Please refer to the Phase 3 announcement and clinical research guidance for details. If you are interested in participating in our Professional Development and Best Practices Group for CRCs, please show your interest by joining our listserv. Coping with nausea and appetite problems 5. Greta Macaire, MA, RD, CSO Lisa Ploss, MPH, RD, CSO, CDE, FADA, FAND UCSF Mount Zion 1600 Divisadero Street, Room B-101 UCSF Mission Bay, Bakar Precision Cancer Medicine Building 1825 4th Street, 4th and 5th Floors Questions that the dietitian may address include: 1. 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). ConsentingPart 1 - Overview of Belmont reportPart 2 - Methods for consent compliance when enrolling subjects, Documentation Patients, family members and caregivers often seek reliable sources to find information. Cardiac Electrophysiology/Arrhythmia Service, Jennifer Ko (Social Activities & Outreach Officer), Marin Thompson (Continuing Education Officer). This educational resource is designed for both new and experienced Clinical Research Coordinators, and other clinical research staff at UCSF who are seeking training resources, including written material, classes and computer based learning modules. The UCSF Neuro-Oncology Caregiver Connection Program connects caregivers of UCSF brain tumor patients to other caregivers for peer support. Human Research Protection Training Overview of the regulations that guide human subject research and what are those responsibilities. Click here to sign up for CRC Bootcamp January 28 and 29, Data Management February 3, and Effective Communications on February 4. DocuSign eConsent Platform is Compliant with FDA Part 11 UCSF now has a version of DocuSign that … Defining the terminology needed for Adverse event documentation. Webinar - additional training sessions have been added for general Q&A and Subject Enrollment. More info on the Training website. Welcome to Human Resources at UCSF and UCSF Health. Orientation, CRC 101 and CRC 102 are focused on basic knowledge that is beneficial for new staff as they start their clinical research career at UCSF. The knowledgeable staff of the Cancer Resource Center has created a series of Patient Education Resource Pages which list credible publications and websites. The CITI Good Clinical Practice (GCP) Basic Course is an overview of GCP. Training. UCSF CRC Training Series: Informed Consent (CRC 101) Print PDF. Some units on campus require this course, but it is optional for the HRPP. If you are a CRC or clinical research support staff: Clinical Research Coordinators (CRCs) are responsible for the organization, coordination, and overall integrity of a research project with humans. The Clinical Research Coordinators (CRC) Council's goal is to serve as an ongoing forum for networking and resource sharing within the clinical research community here at UCSF. Please take a look at our Frequently Asked Questions: FAQs Study Recruitment We are committed to leading HR initiatives and partnering with the UCSF community to attract, develop, and retain the diverse talent necessary to be the world's preeminent health sciences innovator. UCSF Investigators: Katherine Van Loon, MD, MPH, and Geoffrey Buckle, MD, MPH. The eLearning modules are available at any time, and in-person courses are offered periodically throughout the year. All Health Staff, 2. The session also … OnCore Technical Support and Training Team - [email protected] / 415-502-2962; APeX Research Support Team - APeX Research/CRC Page / 415-514-APEX (2739) Training. The first section focuses on the CRC responsibilities, common tasks, and how CRCs will work with UCSF partners in their day-to-day roles. Homemade smoothies are often more healthy than store bought types and can be tailor made to your taste preferences. Phone: 415-502-8046 The listserv server will pull your email address from the FROM field of your email. ©2021 The Regents of the University of California, Clinical Research Coordinator (CRC) Job Series, Principles of Good Clinical Practice (GCP), Part 2 - Methods for consent compliance when enrolling subjects, Association of Clinical Research Professionals, Society of Clinical Research Associates (SoCra), Interactive Training Video (The Research Clinic), Clinical & Translational Science Institute (CTSI). The specific trainings that you require will vary based on what types of clinical research projects you are working on. Please keep checking this site for updated class information. The group is lead by a Council comprised of representatives from a variety of departments. Steps to prepare for and participate in external audits and what comprises audit readiness. CRC Council vision and mission statement 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. The Radiology Clinical Research Coordinators (RC)2 provide the Radiology & Biomedical Imaging Department with a team of personnel who can provide expertise in conducting clinical research studies. In particularly, new CRCs are strongly encouraged to sign up for CRC Bootcamp, which is focused on basic knowledge that is beneficial for new staff as they start their clinical research career at UCSF. The Office of Clinical Trial Activation (OCTA, formerly the Office of Clinical Research) is the centralized one-stop shop for clinical research activation at UCSF, borne out of a goal of streamlining, standardizing, and improving support for the start-up of clinical research activities at UCSF. Discuss paper and electronic copies and the importance of investigator and coordinator documentation effecting audit outcomes, Safety of the Subject – Definitions The CTSI Training team conducts regular, in-person training courses for Clinical Research Coordinators (CRCs) of all levels. For system security and compliance, training is required to gain access to OnCore. The checklist includes various training materials currently available, recommended and as needed items for each type of research (behavioral, observational and interventional). Where indicated, use of resources requires acknowledgement of the CTSI grant. Accelerate is managed by the UCSF Clinical and Translational Science Institute (CTSI).Resources presented are offered by CTSI and other campus units. Reporting Adverse Events We are also working on additional courses to offer later this year. Review of FDA and IRB guidance on recruiting subjects for research. These trainings are sponsored by the Office of Clinical Research (OCR). If you have questions or suggestions, please email [email protected]. Managers - Manage Your Profile. Date Monday, May 21, 2018 - 9:00am to 11:30am. Overview of timeliness for reporting and which agencies are involved. These modules take about 5 hours according to the APEX training staff. Clinical Research is in Phase 3 reopening effective Sept. 17, 2020. Note: These modules can take several days to complete. It is very important that your UC Learning Center profile include updated information like the name of your manager. We support investigators with study set-up and management, CHR and IACUC submissions, and clinical research rates. 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. All CRCs and any clinical research support staff are encourged to join the CRC’s listserv. Study Start Up If you have problems, contact us at [email protected]. Training and mentorship to pre-doctoral students in clinical and translational research methodology and practice. Browse opportunities from didactic coursework to career development awards, and more.. It reviews the basic components of the CRC role at UCSF. Accelerating Research to Improve Health. 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. In particularly, new CRCs are strongly encouraged to sign up for CRC Bootcamp, which is focused on basic knowledge that is beneficial for … We recommend that Coordinators who are new to UCSF visit Resources for New Coordinators for general institutional information. Describes how sponsor monitoring is regulated for quality control and quality assurance of both investigative sites whether industry or sponsor- investigator studies, Preparing for an Audit Problems with co… Orientation This workshop is the beginning class in the series. Frequency: Annually . Offer insight to senior leadership about workflows in order to help strategize training plans for all CRCs. The system also functions as a document repository, providing study personnel with easy access to study documents like approved consent forms. Health and Campus Courses. UCSF is an institution of higher learning where tomorrow’s leaders in the life sciences, health care and health policy receive high-quality education and training. Three UCSF researchers have received New Innovator Awards from the National Institutes of Health to help fund their "moon shots." Please review the recently posted Clinical Research Coordinator (CRC) Job Series. Home > UCSF Compliance* and Most Requested Training. Nutrition guidelines for specific cancers 3. Vision Statement: To help CRCs achieve success at UCSF by being champions for clinical research. Identify and disseminate best practice information within the CRC community. Training for Clinical Research Coordinators In-person and eLearning courses are available for UCSF Clinical Research Coordinators (CRCs) and study team members. Good Clinical Practice (GCP) Information IRB’s online submission and review system for research studies. Sponsor Responsiblities Physician, Nurses and Licensed Independent Contractor (Clinical Staff) ... Health Staff - HOD, PCA, CRC, etc. About Us: We are a diverse group of clinical research professionals who promote cross-functional collaboration for research initiatives at UCSF. Caregivers are matched, as best as possible, by tumor type, treatment, age and family situation so that family and friends can talk to someone who best understands their new caregiving circumstances. The group is lead by a Council comprised of representatives from a variety of departments. The CTSI Training team conducts regular, in-person training courses for Clinical Research Coordinators (CRCs) of all levels. Support students transitiong into a clinical research job The person may receive training and development to prepare and advance for journey-level work at the next level within the series. Clinical Research Coordinators Council Classes: There are no new classes scheduled at this time. Training is required for personnel working with human source material (including established or primary cell lines, blood, body fluids, organs, and tissues), or are members of a PI’s laboratory who has BUA approval to work with any human source materials. APeX training for Clinical Coordinators Best practice considerations when opening a new study to avoid management problems. Infection Control Training * Audience: 1. 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. 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