Staff Specialist Institutional Review Board Institute University of Utah
The Trusted Standard in Research, Ideals, Compliance, and Safety Preparation
The Collaborative Institutional Preparation Initiative (CITI Program) is dedicated to serving the grooming needs of colleges and universities, healthcare institutions, technology and research organizations, and governmental agencies, as they foster integrity and professional advancement of their learners.
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- Research
- Ethics
- Compliance
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- Other Offerings
Infection Prevention in Healthcare Settings
Featured New
Provides learners with a foundational understanding of infection prevention techniques.
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Laser Prophylactic
Featured New
Meets the requirements of a general laser safety training program for inquiry and medical institutions.
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General Laboratory Safety for Non-Laboratory Personnel
Featured New
Hazard awareness, communication, and safe practices for non-lab personnel working in and around laboratory facilities.
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Understanding 483s and Surviving Them
Featured New
Discusses steps that investigators and clinical sites can take to empathise and respond to an FDA Course 483.
Open Access Publishing: An Introduction
Featured New
Provides an overview of open access publishing, covers mutual challenges to copyright and licensing, and discusses impact and equity within academia.
Preparing to Publish in Traditional and Hybrid Journals
Featured New
Covers key concepts in scholarly publishing and provides an overview of the publication process for both traditional and hybrid...
Data Management and Security for Student Researchers: An Overview
Featured New
Covers the all-time practices of data management and security for graduate student researchers.
Bring Your Own Device (BYOD) Studies
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Discusses BYOD report best practices, implementation, and Institutional Review Board (IRB) review.
Good Manufacturing Practices (GMP)
Featured
An in-depth introduction to GMP for pharmaceuticals.
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Protocol Evolution and Execution: Across a Concept
Featured New
An in-depth review of the development and execution of protocols.
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Technology Transfer
Featured
An introduction for researchers on university applied science transfer and commercialization processes.
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FDA Inspections: From Site Preparation to Response
Featured
Covers regulatory inspections of clinical investigators and sites, including mock inspections, 482s, 483s, warning letters, communication, and CAPA plans.
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Working with Your IRB
Featured
Strategies to piece of work with your reviewing IRB.
Facial Recognition Considerations for Researchers
Featured New
Covers the use of facial recognition systems in research and healthcare.
Communicating Research Findings
Featured
This grade focuses on effective practices, guidelines, and strategies for communicating and presenting enquiry findings.
Family Educational Rights and Privacy Act (FERPA)
CME/CEU Featured
This course covers the core requirements of the federal Family Educational Rights and Privacy Act (FERPA).
Healthcare Ethics Committee (HEC)
CME/CEU Featured
This form focuses on developing the knowledge and skill base necessary for being a successful healthcare ethics committee member.
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Responsible Conduct of Research (RCR) Basic
CME/CEU Featured
This class covers the core norms, principles, regulations, and rules governing the do of research.
Title IX and the New Regulations
Featured
Discusses central elements of the new 2020 regulations, how they bear on the institutional community, and what you should know to implement best practices into revised Title IX procedures and policies.
IRB Protocol Noncompliance: When Research Goes Rogue, What Next?
Featured New
Discusses strategies to address researcher noncompliance with IRB-approved protocols.
Radiation Safety
Featured New
A detailed review of radiation rubber for research and medical institutions.
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Undue Foreign Influence: Risks and Mitigations
Featured
Explore key ethical, export, security, intellectual holding, and transparency requirements related to international appointment.
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False Claims Act: A Primer and Guide for Enquiry Organizations
Featured
This course provides an introduction to the False Claims Act ideally suited for faculty, researchers, and staff at research organizations.
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Bounty Reporting (Attempt Reporting)
Featured
A focused discussion for individuals who piece of work with federally sponsored awards, PIs, and other members of the research squad.
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Preparing for Success in Scholarly Publishing
Featured New
Foundational course that orients and prepares learners to engage with the scholarly publication procedure in an informed way.
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A Beginner's Guide to Being a Sponsor-Investigator
Featured New
A primer for understanding the sponsor-investigator role and responsibilities in clinical research.
Partnering with Technology Companies
Featured New
Provides an overall approach to and all-time practices for partnering with technology companies to design and comport enquiry.
Educational activity and Grooming for Professionals
Featured
Provides instruction on how to improve your educational activity and training skills in a diversity of settings.
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Disaster Planning for the Research Enterprise
Featured Updated
This course offers data well-nigh disaster planning and business organization continuity to those responsible for research oversight.
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Essentials of Inquiry Administration
CME/CEU Featured Updated
This course provides an overview of research assistants.
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CTrials by BRANY
Featured
CTrials helps grow sponsored research programs by taking on the many administrative challenges inherent in managing clinical trials.
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Protocol Builder
Featured
Protocol Builder is an online protocol writing and collaboration platform that as well speed upwardly your pre-review turnaround times.
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The Network of Networks (N2)
Featured
N2 is a not-for-profit alliance of Canadian research networks and organizations working to heighten national clinical research adequacy and chapters.
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BIC Study Foundation
Featured
BIC Study Foundation is a resource for those who desire to accept CITI Program courses in Korean. They are a certified training provider by the Korean FDA/MAFRA for HRPP and ACU Programs.
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Our Courses
Meet A Few Of Our Skilful Authors and Presenters
Our courses are built by over 150 highly qualified experts and rigorously peer reviewed to comprise various perspectives and ensure accuracy, abyss, and overall quality.
Lauren Danridge serves as the Acquaintance Director, ACUO at the University of Michigan, assisting in the leadership and management of oversight the program, reducing regulatory burden, making programmatic improvements, and streamlining business processes to increase efficiency and effectiveness. Lauren has over 20 years experience in laboratory creature research and compliance.
Cheryl has over 30 years of experience in human research protections, serving both the civilian and armed forces arenas. She has been an author/editor for CITI since 2002, serves on a number of PRIM&R groups, and has been an invited presenter at numerous national and international venues.
Mariette Marsh is the Assistant Vice President, Regulatory Affairs and Rubber at the University of Arizona. She holds a masters degree in public policy and is certified in IRB, HIPAA, and hospital research compliance. She serves as a site reviewer for the Association of Accreditation of Human Inquiry Protection Programs (AAHRPP).
Andy Coravos is the CEO/co-founder of Elektra Labs, edifice a digital medicine platform for decentralized clinical trials. She serves as a enquiry collaborator at the Harvard-MIT Center for Regulatory Sciences. Formerly, she served equally an Entrepreneur in Residence at the FDA. She serves on the Board of DiMe.
In Our Learners' Words
Myrene Chiliad.
Associate Kinesthesia
The form materials are brief and clear. Such brevity and clarity are perfect for those who are busy with other duties at work and provide for a more friendly and less overwhelming task. I love the quizzes because I can acquire from my mistakes. Afterward submitting the quiz, the correct and wrong answers are explained. This reinforces learning.
Julie S.
Assistant Professor & Postdoctoral Enquiry Fellow
These courses were easy to access and succinct, which made a review of the Belmont Report primal tenets, as well as the review of differences between do and inquiry, a focused and fourth dimension efficient endeavor.
Folasade A.
Educatee
I similar the opportunity to be able to read/review CITI study notes at any time.
Motunrayo O.
Professor
Very educative course. Information technology was insightful and informative. I learned and relearned a lot.
Courses Approved by a Top Bookish CME Provider
CITI Program courses are approved for CME credits through the Albert Einstein Montefiore Continuing Professional Development Center (CPDC).
Albert Einstein Higher of Medicine-Montefiore Medical Eye (Einstein) is accredited by the Joint Accreditation for Interprofessional Continuing Teaching to provide continuing education activities for healthcare professionals. Einstein is accredited to offer continuing educational activity credit for the following professions: medicine, nursing, psychology, chemist's shop, and social work.
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Contempo News & Manufactures
Content Update News
New Course – Infection Prevention in Healthcare Settings
This course provides learners with an understanding of pathogen manual in healthcare settings, current scientifically accepted infection prevention principles, and prevention strategies that minimize pathogen transmission amid patients and healthcare personnel.
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Blog
What CITI Programme is Reading – April 12, 2022
"What CITI Program is Reading" is our weekly blog series which highlights news articles curated by our staff and relevant to enquiry, higher education, healthcare,...
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Upcoming Events
Costless Alive Webinar – Best Practices for Global Research Partnerships: Benefits and Challenges
Nosotros will talk over the importance of global instruction and practice in international enquiry to ensure the priorities of local partners sets the agenda for our work.
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Source: https://about.citiprogram.org/
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