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All-Access Webinar Package Now Available to ATSU Faculty & Staff|
ATSU's Division of Research, Grants, and Scholarly Innovations is pleased to announce we have expanded our subscription with CITI (Collaborative Institutional Training Initiative) to include the All-Access Webinar Package! These webinars are now available for access at no additional cost to interested ATSU faculty and staff members. Instructions for Accessing CITI Webinars The All-Access Package includes at least 46 webinars on a wide variety of topics, including: |
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Ethics & Policy Issues in CRISPR Gene Editing COVID-19: Supporting Ethical Care and Responding to Workforce Concerns in a Public Health Emergency Race in Clinical Research: Ethics and IRB Decision Making Informed Consent and Clinical Investigations: A Focus on the Process Remote Informed Consent: The Same, but Different, but Still the Same Informed Consent and Research with Wearable Tech Understanding Decentralized Clinical Trials (DCTs) and Virtual Study Visits Decentralized Clinical Trials (DCTs) and Your Workforce The Challenge of Medicare Advantage Plans and Local Coverage Determinations Export Compliance: An Overview for Staff, Students, and Faculty Remote Contact Tracing Basics for COVID-19 Investigating and Tracing a Case’s Contacts Contact Tracing Ethics and Responsibilities Getting Started in Grant Writing: An Introduction for Graduate Students, Postdocs, and New Faculty Cost Allowability on Federally Sponsored Awards |
Managing Conflict with Your Dissertation Chair International Students in Focus at U.S. Higher Education Institutions (HEIs) Title IX and the New Regulations Accreditation 101 for New and Adjunct Faculty Principles and Practices for Managing Undue Foreign Influence in an Academic Environment Blockchain and Higher Education Participating in Vaccine Research Research with Native American Communities: Important Considerations When Applying Federal Regulations Preparing for Single IRB (sIRB) under the Common Rule Running a Virtual IRB Meeting Nuts & Bolts of Running a Virtual IRB Meeting Medical Marijuana: A Budding Field of Research Understanding Consent Requirements and “Key Information” Under the Revised Rule Health Disparities: Promoting Equity and Diversity in Clinical Research Artificial Intelligence (AI) and Human Subject Protections Social Media and Research Recruiting COVID-19 and Human Research Protection Programs |
Working with Your IRB IRB Administrator Professional Development and Self-Advocacy GDPR & Human Subject Research in the U.S. GDPR: Top Noncompliance Risks and Mitigation Strategies FERPA: A Quick Review of the Law for Researchers and IRBs FERPA and Online Learning in the Time of COVID-19 Building a ClinicalTrials.gov Importance of Peer Review and Data Validation in Research Transitioning Research to the Revised Common Rule: The What, How, and Why Revised Common Rule: Overview of Revisions Revised Common Rule: Revisions to Definitions Revised Common Rule: Revisions to Informed Consent Intellectual Property and Working With Your Technology Transfer Office The Playbook: Successfully Developing and Deploying Digital Clinical Measures |