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Grants & You Fall 2021: CITI Webinars

  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:

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 Compliance Program – Tips for Investigators and Institutions

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