Now I know the computer program Epic (APeX) like the back of my hand and I am learning the details of ATRT diagnosis and treatment using the Children's Oncology Group ACNS0333 protocol. Alternatively, you may have mistakenly bookmarked the MyAccess login form instead of the actual web site you wanted to bookmark, or used a link created by somebody else who made the same mistake. The target audience is advanced CRCs that have completed studies involving auditing, or those who may experience auditing activities. Do not submit directly to the APeX team. CRC 104: Effective Communications for CRCs                   Thursday, February 4, 8.30am - noon. Informed Consent is a critical part of the CRC role. Where indicated, use of resources requires acknowledgement of the CTSI grant. Here's everything you need to know to: Select types of content for the site; Create new content; Zion. For instructions on linking encounters, please reference the APeX User Guide for UCSF Clinical Research Coordinators (CRCs). Plan ahead for integrating with APeX. Help. Contact us. CRC Orientation                                                                      Thursday, January 28, 8.30am - 11am. This course focuses on the purpose and process for monitoring and audits in clinical research. Overview; Projects; Announcements; Resources; ZSFG QI Corner; Reporting Apps. New Online Resource: UCSF COVID-19 Related Research June 4, 2020. ... Primary CRC Name: This should be the main contact for the study and/or the CRC responsible for billing review. Three UCSF researchers have received New Innovator Awards from the National Institutes of Health to help fund their "moon shots." Design work started in earnest in July 2010. Please read: 1. OCR team provides CA . If non-CRB, who approved as non-CRB? Audience: Current CRCsPrerequisites: CRC Bootcamp, CRC 201: Audit Readiness                                                     next course date tbd. Register here for the May 15th event. Evaluation of diagnostic tests and treatment efficacy in clinical settings, Risks associated with using, transmitting, and storing electronic information, How to maintain the confidentiality, integrity, and availability of data, Roles and responsibilities of each community member in protecting UCSF's data and systems. CRC 202: Protocol Training, MOPs & SOPs                         next course date tbd. Build study in Apex. The session also introduces resources such as the HUB and IRB website. It reviews the basic components of the CRC role at UCSF. UCSF at Mission Bay; UCSF at Mount Zion; UCSF at Parnassus; VA Medical Center; Zuckerberg San Francisco General Hospital and Trauma Center; Clinical Resources; Quality & Safety. UCSF at Mission Bay; UCSF at Mount Zion; UCSF at Parnassus; VA Medical Center; Zuckerberg San Francisco General Hospital and Trauma Center; Clinical Resources; Quality & Safety. UCSF's NLP community curates knowledge as participants experiment, learn and implement NLP tools in clinical and biomedical research projects. If you are a supervisor, contact us at 415-437-1600. www.ucsf.cprcpr.com If you are not sure about billing, contact your supervisor. Audience: CRCs with some study experience.Prerequisites: CRC Bootcamp (Orientation, CRC 101: Informed Consent, CRC 102 IRB & Safety Reporting) is highly recommended. Anesthesia QI Reporting; ZSFG QI Reporting; Divisions. ©2021 The Regents of the University of California, UCSF Health Annual Infection Control Training for Ancillary Staff, San Francisco Veterans Affairs Medical Center (VAMC), Zuckerberg San Francisco General Hospital (ZSFG), Get help with the new processes for Track More with OnCore, Orientation - Thursday, January 28th, 8.30am - 11am, CRC 101: Informed Consent - Thursday, January 28th, 11am - 3pm (includes a break for lunch), CRC 102: IRB & Safety Reporting - Friday, January 29th, 8.30am - noon. Frequency: Every two years This course will describe how to identify if your study requires an IND, types of INDs, and the scope of the application process. CRC/research staff training and support: Our clinical research staff requires training in infection control and COVID-19 … Read. Study Type. 07Feb19. Getting Full-Text Access Getting Access to UC-Licensed Resources; Using the EZproxy Bookmarklet; Alternative Access: How to Get the PDF? You are cordially invited to the 2nd Annual Clinical Trials Day at UCSF! Explore resources, expertise, and best practices for: Who You Are. This course is especially applicable for those working on NIH-sponsored Investigator-initiated clinical trials or studies where UCSF is the coordinating center. Paul Asfour offered to … Remember to have your own study consents for practice (or we will provide if you don’t have one). If you are not with UCSF, you can view our upcoming classes here: www.cprpcr.com If you are with UCSF and you are in an approved department (Nursing, Ambulatory or Respiratory), you can register here. If you need an account, ask your manager or school to request an account for you or contact us, and we'll set you up. The second section explores job basics including Best Practices for Documentation, Data Security, IRB, Coverage Analysis and the concept of Study Start Up. The post-award section covers ZZ statements and research billing with a focus on coverage analysis and its impacts on the research process. APeX New Clinical Trial Study Request Form Study Name, beginning with ZZxxxx, Study: ... clinicaltrials@ucsf.edu for processing. The courses are focused on basic knowledge that is beneficial for new staff as they start their clinical research career at UCSF. It will also discuss how to handle IND modifications, safety reports and annual reports. The course will highlight best practices for data design, management and analysis as well as how to implement processes for quality assurance and quality control. Incident Response For documenting, tracking, and facilitating the resolution of Information Security incidents. The infrastructure for UCSF Clinical Systems is a complex enterprise environment so you’ll need to … APeX New Clinical Trial Study Request Form . The pre-award section of this class covers study start-up and finance topics important to CRCs conducting interventional research studies using APeX and OnCore for billing procedures. Submitted by ucsf_admin on Mon, 09/09/2019 - 14:41. The CRC’s website cancer.ucsf.edu/crc features new patient and caregiver Powerpoint orientations in Tagalog, Mandarin, Cantonese, Korean and Vietnamese – Margaret Gray; Nicole (Heme BMT charge nurse) has need for getting teaching sheets and consents translated. Attention: This page is only for UCSF staff in approved departments to register for a class. Leave plenty of time in your efforts for governance and approvals. We will describe best practices and provide checklists and activities to help you prepare in the event of an audit. Hit enter to search. Anesthesia QI Reporting; ZSFG QI Reporting; Divisions. This event is sponsored by the UCSF Office of Clinical Research. Audience: New and current CRCs.Prerequisites: Human Subjects and GCP via CITI. Design Study Set Up Study Conduct Study Audience: New or current CRCs.Prerequisites: none, CRC 105: The Investigational New Drug Process                Online | On-demand. More topics are in development! The IND Process is available on the UC Learning Center - to take it, either login to MyAccess and follow the link for Learning Management System, or follow this link. Additional topics include the Informed Consent Process and Documentation. General Compliance Briefing: University of California Ethical Values and Conduct. The target audience is new UCSF employees, but anyone who would like a refresher is welcome to participate. Class schedule (all courses conducted on Zoom): NOTE:  you must use your UCSF email address to register; registering for Bootcamp enrolls you in Orientation, CRC 101, and CRC 102 - please do NOT also enroll in the individual courses. The first section focuses on the CRC responsibilities, common tasks, and how CRCs will work with UCSF partners in their day-to-day roles. • The list includes 797 Clarity reports and 446 Reporting Workbench(RWB) reports. Guidance for Category 2 and 3 Research Conducted “Offsite”, Outside of UCSF-Affiliated Facilities June 26, 2020. CA and 2. Once you are in the "Find a Course" section, search for "Investigational New Drug Process". All lab results, radiology results, and other clinical information from July 1, 2005 onward was in UCare until the information was transistioned to APeX in 2012. Cu rrently Admin's don't have access to the Clinic Schedules and while some clinic schedulers have general access to faculty calendars, they cannot see up to minute changes in availability entered by Admins or Faculty.. Linking patients in APEX . The UCSF Radiology eUnity / WebPACS system is a web-based image distribution solution where the viewer is called up through a browser. CRC 103 In this interactive class we will demonstrate and practice performing an informed consent. Stage of Research. CHR # / CAR # (Study Code) Chart of Accounts (COA) Dept ID (6-digits) - Fund (4-digits) - Where indicated, use of resources requires acknowledgement of the CTSI grant. Study Name, beginning with ZZxxxx, Study . Please join us for Bootcamp, which includes Orientation, CRC 101: Informed Consent,  and CRC 102: IRB & Safety Reporting. The Bakar Institute sponsors several organized workshops throughout the year, partnering with various internal and external organizations to deliver key trainings in computational health sciences: Department of Epidemiology & Biostatistics Training has offerings for all career phases include individual courses, certificate programs, graduate degrees and postdoctoral fellowships: Library Data Science Initiative offers workshops, programs and expertise/office hours in: Security Awareness and Training. Clinical Research Return to Work Checklist (updated 8/17/20) June 5, 2020. You are cordially invited to the 2nd Annual Clinical Trials Day at UCSF! This workshop is the beginning class in the series. UCSF Discounts & Specials, Entertainment, Fitness Centers, Outdoor Recreation, Special Events Fitness & Wellness Membership, Schedules, Class Sign-up, Healthy Living The eLearning modules are available at any time, and in-person courses are offered periodically throughout the year. Bakar Computational Health Sciences Institute Workshops. The implementation process gained speed when Pamela Hudson, executive director of clinical systems at the medical center and program director for APeX, came on board at UCSF in April 2010. ApeX, (Advanced Patient-Centered Excellence), is UCSFs electronic EPIC based, Medical Record System (EMR) and electronic health record (EHR) system which puts increased emphasis on patient safety and medical error prevention by creating one electronic patient chart thats accessible across the institution, increasing the continuity of care. This course will describe the origin, flow and management of data through a clinical study, and the specific role of the CRC in each phase of the process from data design to analysis & reporting. This class will review Adverse Event (AE) recording best practices, including a demonstration of a participant interview with break-out time for all to practice. This campus directory is the property of the University of California San Francisco. The UCSF Helen Diller Family Comprehensive Cancer Center (HDFCCC) is a national leader in oncology research. Effective Communications are an essential component of protecting participant privacy, confidentiality, and for developing positive relationships with your participants, supervisor, colleagues and University-wide. Discuss how Official cost estimate is obtained after initial CA is approved by PI. We highly recommend that new CRCs attend both days for completion of all courses. You may be seeing this page because you used the Back button while browsing a secure web site or application. The latest — and biggest — APeX rollout this month was the culmination of a process that began in December 2009. How Do I Get APeX on My Computer or Mobile Device? Resources presented are offered by CTSI and other campus units. I'm suggesting a system that will:. Audience: New CRCs under 6 months.Prerequisites: Review the HUB including Suggested Training List, HIPAA 101 and Human Subjects via CITI. In this course we will discuss best practices for communicating with your participants, supervisors and partners at UCSF. UCSF Informatics Day 2014 - Sayan Chatterjee, "APeX Reporting" 1. Get up to speed on: [email protected]. Protocol Training, MOPs & SOPs is an advanced series course that reviews protocol training fundamentals, manual of procedure (MOP) & standard operating procedure (SOP) functions and best practices for creation and maintenance thereof. Investigators Study Staff Participants. Register here for the May 17th event. CRC 106: Data Management for CRCs                                 Wednesday, February 3, 8.30am - noon. Clinical Research Announcement: Return to Work and Checklist. Perform Billing Review. UNIVERSITY COLLEGE SABAH FOUNDATION Jalan Sanzac, 88100 Sembulan Kota Kinabalu, Sabah Tel : 088 – 511 111 Fax : 088 – 511 100 enquiry@ucsf.edu.my NOTE: there is no need to register for individual courses if you have registered for Bootcamp, CRC 101: Informed Consent                                                  Thursday, January 28, 11am - 3pm. Content is what we're all about – and as Content Owners, you make it happen. Pharmacy students stepped up to the COVID-19 response by administering UCSF's first vaccines to frontline workers. Subject Recruitment and Enrollment Please visit the Clinical Research Resource HUB for appropriate strategy of effectively enrolling subjects. Accelerate is managed by the UCSF Clinical and Translational Science Institute (CTSI). Thank you! By housing all patient information in one electronic database, it eliminates the duplication of tests, sends alerts to warn of allergies to medications or contradictions an… Safe in-person classes are a … This is the same viewer used by APEX when users click on the url to "Show images for ..." the imaging exam selected by the user. Audience: Experienced CRCs who have been in their role for at least 1 year.Prerequisites: CRC Bootcamp Series (recommended). Scheduling and APeX Orders Before scheduling can begin, please ensure that you have submitted the Full Study Application. ©2021 The Regents of the University of California, User Guide for Clinical Research Coordinators, COVID-19 Electronic Health Data for Research, Bakar Computational Health Sciences Institute Workshops, Department of Epidemiology & Biostatistics Training, Clinical & Translational Science Institute (CTSI), The latest information for CRCs, including a tip sheet with instructions on which Learning Management System CRC Courses, is located on the, For a useful tip sheet on using APeX in clinical research studies, including information about coverage analysis and billing review, please see. UCare was the electronic medical record for Moffitt-Long Hospital, the Parnassus Ambulatory clinics, Lakeshore, and Mt. Full Study Title. Benefits of using the UCSF API Portal Open Up Your Data to UCSF Developers. Maximum length is 25 characters. The collaborative effort of all stakeholders has caused the UCSF Medical Center bill hold to be substantially reduced, although work remains. If the study has a Chart of Account (COA) Change, please provide a new Effective Date. APeX An electronic health record across all care settings at UCSF Medical Center, UCSF Benioff Children's Hospital and more than 130 UCSF clinics. There is a disconnect between the Academic and Clinic Patient Calendaring. This course will summarize resources available at UCSF. Audience: All Campus and Health employees except those who are part of the COIR requirement or those typically exempted such Emeritus or WOS. Study Description . You must first “Sig… APeX Reporting Overview Sayan Chatterjee APeX Reporting Manager June 06, 2014 1 2. CRC Bootcamp (Orientation, CRC 101, CRC 102)               Thursday, January 28 and Friday, January 29. CRC 103: Pre & Post Award Tasks for CRCs                       next course date tbd. Stale Request. 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. Accelerate is managed by the UCSF Clinical and Translational Science Institute (CTSI).Resources presented are offered by CTSI and other campus units. As of January 12 th , there were changes to the APeX workflow for Clinical Research Coordinators, designed to reduce the burden on study teams and to improve billing compliance. To request changes to a department listing please open a ticket at help.ucsf.edu, or contact the IT Service Desk at (415) 514-4100. After the setup of a study is complete, managing the study procedures involves a series of steps listed below. The class will also discuss IRB reporting requirements including the following: AE/SAE Reporting, Post Approval Reporting and Subject Injury. Audience: New or current CRCs with responsibilities on Interventional Studies.Prerequisites: none. 2 Reports in production by numbers • There are 1350 reports available in APeX production right now. December 01, 2020 15:44. NOTE: please do NOT register for individual courses if you registered for Bootcamp; you must use your UCSF email to register, CRC 102: IRB & Safety Reporting                                         Friday, January 29, 8.30am - noon. Reiterate how CA is the first step in billing review and drives all CRC tasks going forward. Open Monday through Friday from 9 am to 5 pm: 415.885.3693 (voice) 415.885.3701 (fax) Email Us The Patient and Family Cancer Support Center (Mission Bay) Bakar Precision Cancer Medicine Building Barbara and Richard Rosenberg Cancer Resource Suite 1825 Fourth Street, First Floor San Francisco, CA 94158 The Ida and Joseph Friend Patient and Family Cancer Support Center (Mount Zion) 1600 Divisadero St., B-101 San … You will know when someone wants to use your API as you will receive an access request. Have more questions? CRC 101: Informed Consent - Thursday, January 28th, 11am - 3pm (includes a break for lunch) CRC 102: IRB & Safety Reporting - Friday, January 29th, 8.30am - noon; NOTE: you must use your UCSF email address to register; registering for Bootcamp enrolls you in Orientation, CRC 101, and CRC 102 - please do NOT also enroll in the individual courses. In-person and eLearning courses are available for UCSF Clinical Research Coordinators (CRCs) and study team members. Please be ready to participate! Audience: New and current CRCs.Prerequisites: HIPAA 101, Human Subjects and GCP via CITI, and Research Integrity Video. This event is sponsored by the UCSF Office of Clinical Research. Audience: New or current CRCs with responsibilities on interventional studies.Prerequisites: Review the Start-Up Diagram and the APeX Job Aid on the HUB. You must first have a UCSF APeX account. Overview; Projects; Announcements; Resources; ZSFG QI Corner; Reporting Apps. Online Help Keyboard Shortcuts Feed Builder What’s new All courses are free of charge. If there is a particular subject you would like to see covered in a course, or if you have any other questions about the CRC Training program, please contact Lisa Schoonerman via email, or at 415-514-8403. Clara Wu Project: Retrospective Outcome Review of Patient's with … Attention new CRCs! This site will work best on a computer – not a mobile device. ... (CRC), and the Gamete, Embryo and Stem Cell Committee (GESCR). 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