Webinars

The webinar library is the newest addition to CITI Program's offerings.

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About the Webinars

CITI Program offers webinars that reflect current topics important to our subscribing organizations and independent learners. These topics come from the range of CITI Program’s catalog of courses and are presented by experts.

Learn more about the All Access Webinar Package, available only to subscribing organizations for an annual fee.

Language Availability: English

Suggested Audiences: Billing/Coding Staff, Bioethicists, Clinical Research Coordinators, Clinical Researchers, Compliance Professionals, Department Administrators, Faculty, Higher Education Administrators, Institutional Review Board (IRB) members, Institutional/Signatory Officials, International Student Supervisors, International Students, IRB Chairs, IRB/HRPP Administrators and Staff, Principal Investigators, Privacy Officers, Registration Staff, Research Administrators, Research Team Members, Researchers, Sponsors, Students


Multiple Webinar Packages

All Access Webinar Package (Organizations Only)

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Provide your organization's learners with access to currently available and future webinar recordings.

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Diversity Training in Clinical Research Webinar Package (Organizations Only)

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Provide your organization's learners with access to webinars that cover diversity issues in clinical research.

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Animal Care and Use Webinars

Noncompliance and the IACUC: Basic Approaches for Success

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Explores various types of noncompliance and their impact.

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Bioethics Webinars

Human Enhancement and its Ethical Implications

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Explores the topic of human enhancement and the ethical considerations it presents.

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Ethics & Policy Issues in CRISPR Gene Editing

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Explore the ethical and policy issues that CRISPR gene editing presents in this engaging webinar.

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COVID-19: Ethical Care and Workforce Concerns

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This webinar reviews public health duties, challenges with resource allocation, management of work conditions, workforce response, and effectively collaborating with regional hospitals.

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Race in Clinical Research: Ethics and IRB Decision Making

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Explores the concept of race in clinical research and important ethical and regulatory questions.

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Clinical Research and GCP Webinars

Working with the FDA: Medical Devices and Regulatory Touchpoints

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This webinar discusses practical and strategic approaches to interacting with FDA during medical device development.

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FDA Inspections of GMP Facilities: How to Be Inspection Ready

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Discusses the FDA’s approach to inspecting GMP facilities and the ways that facilities can prepare for inspections.

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CRA Soft Skills, Time Management, and Effective Site Relationships

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Discusses the importance of CRA soft skills in building productive relationships with sites and sponsors.

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Understanding 483s and Surviving Them

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Discusses steps that investigators and clinical sites can take to understand and respond to an FDA Form 483.

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Research Equity and the Part We Play

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Discusses ways to improve diversity and equity among clinical trial participants.

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Improving the Clinical Trial Participant’s Experience

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Discusses ways that sponsors, sites, and clinical research organizations can transform the clinical trial experience.

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ClinicalTrials.gov Enforcement: An Update

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Explores recent FDA enforcement of FDAAA 801 and noncompliance pitfalls to avoid.

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ClinicalTrials.gov & Building A Compliance Program

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Review reporting regulations, learn about noncompliance, and discuss how to build a successful compliance monitoring program.

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Informed Consent and Clinical Investigations: A Focus on the Process

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Explores current challenges and improvement strategies related to informed consent.

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Remote Informed Consent: The Same, but Different, but Still the Same

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Presents remote consent considerations and scenarios.

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Informed Consent and Research with Wearable Tech

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Explore informed consent issues with wearable tech research.

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Understanding Decentralized Clinical Trials (DCTs) and Virtual Study Visits

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Introduces DCT models and components, and provides best practices for virtual study visits.

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Decentralized Clinical Trials (DCTs) and Your Workforce

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Explores changes to the site’s workforce including updates to traditional roles and new positions and skills needed for DCTs.

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A Beginner’s Guide to Being a Sponsor-Investigator

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A primer for understanding the sponsor-investigator role and responsibilities in clinical research.

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Clinical Trial Billing Compliance Webinars

The Challenge of Medicare Advantage Plans and Local Coverage Determinations

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Learn about challenges with drug and IDE studies, variances in local coverage determinations, and how to avoid denials.

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Export Compliance Webinars

Export Compliance: An Overview for Staff, Students, and Faculty

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Provides faculty, staff, and students with an overview of U.S. export control regulations and their application to various activities within institutions of higher education.

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Grants Webinars

Managing Your Grants as Systems: A Guide for Grant Management Success

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Covers a systems approach to grant management and provides strategies for managing your team and your grant.

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Getting Started in Grant Writing: An Introduction

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Learn more about grants, where to find them, and how to submit proposals.

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Cost Allowability on Federally Sponsored Awards

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A review of allowability of expenditures on federally supported projects.

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Higher Education Webinars

Addressing and Understanding Mental Health Challenges for Faculty and Staff

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Provides learners with an overview on the state of faculty and staff mental health while explaining the role an institution can...

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How to Implement Trauma-Informed Care: An Introduction

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Introduces trauma-informed care for implementation with clients, patients, and students.

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A 21st Century Approach to ADA Compliance: Equity and Access

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Provides learners with practical tips to make ADA, Section 504, and accommodations in the 21st century more accessible and equi...

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Best Practices for Global Research Partnerships: Benefits and Challenges

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Reviews best practices and challenges for navigating collaborative research partnerships in a global environment.

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Open Access Publishing: An Introduction

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Provides an overview of open access publishing, covers common challenges to copyright and licensing, and discusses impact and equity within academia.

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Preparing to Publish in Traditional and Hybrid Journals

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Covers key concepts in scholarly publishing and provides an overview of the publication process for both traditional and hybrid...

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Understanding and Addressing Mental Health on Campus

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Reviews the current challenges and opportunities to address mental health at higher education institutions from a public health...

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Managing Conflict with Your Dissertation Chair

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Learn ways to manage conflicts with your dissertation chair and committee.

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International Students in U.S. Higher Ed

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Discusses the different visa types pertaining to international students in the U.S. and their effect on how your students can work, volunteer, and conduct research on and off campus.

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Title IX and the New Regulations

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Discusses key elements of the new 2020 regulations, how they affect the institutional community, and what you should know to implement best practices into revised Title IX procedures and policies.

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Accreditation 101 for New and Adjunct Faculty

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Learn about the importance of accreditation and the role you may plan in your institution’s annual accreditation renewal process.

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Principles and Practices for Managing Undue Foreign Influence

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An introduction to foreign influence concerns, disclosure practices, and recent government directives.

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Blockchain and Higher Education

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An introduction to blockchains and their potential for higher education.

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FCPA and University Research: What Faculty and Administrators Need to Know

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Reviews FCPA as it relates to university research.

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Data Management and Security for Student Researchers: An Overview

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Covers the best practices of data management and security for graduate student researchers.

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Human Subjects Research Webinars

IRB Protocol Noncompliance: When Research Goes Rogue, What Next?

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Discusses strategies to address researcher noncompliance with IRB-approved protocols.

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Research with Native American Communities

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Learn about tribal sovereignty and how to respect the indigenous perspective when planning, conducting, and reviewing research ...

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Preparing for Single IRB (sIRB) under the Common Rule

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Dive deep into the sIRB requirement under the revised Common Rule.

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Running a Virtual IRB Meeting

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Explore different elements associated with running an IRB meeting in a virtual environment, including key areas for IRB chairs, members, and staff.

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Nuts & Bolts of Running a Virtual IRB Meeting

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This webinar explores aspects of virtual IRB meetings including the benefits, technical setup, documentation, and additional considerations such as implementation during a disaster.

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Medical Marijuana: A Budding Field of Research

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Discuss unique challenges and issues as well as considerations for IRB review and steps for getting started in medical marijuana research.

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Understanding Consent Requirements and “Key Information”

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Explore the informed consent requirements related to increasing understandability and “Key Information."

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Health Disparities: Promoting Equity and Diversity in Clinical Research

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Provides an overview of health disparities while raising awareness of this issue in research design and conduct.

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Artificial Intelligence (AI) and Human Subject Protections

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Explores the current protections, regulatory elements, and ethics tools associated with protecting human subjects in light of AI research.

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Social Media and Research Recruiting

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Discusses social media use in research recruiting.

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COVID-19 and Human Research Protection Programs

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This webinar reviews how a human research protection program (HRPP) responded to and dealt with the COVID-19 pandemic.

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Working with Your IRB

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Strategies to work with your reviewing IRB.

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Leveraging IT Insight in IRB Review

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Discusses why technology-based expertise is critical to human subject protections and how to add IT insights to IRB review.

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IRB Review of Observational Research

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Explores different types of observational research and provides best practices for IRB review.

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Research with Mobile Data Collection Tools

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Explores a research team’s experience using mobile audio-visual recording devices in sensitive settings.

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U.S. DoD Regulations & Requirements for Human Subject Research

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Reviews DoD requirements and limitations for research.

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Bring Your Own Device (BYOD) Studies

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Discusses BYOD study best practices, implementation, and Institutional Review Board (IRB) review.

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Partnering with Technology Companies

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Provides an overall approach to and best practices for partnering with technology companies to design and conduct research.

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Information Privacy and Security Webinars

GDPR & Human Subject Research in the U.S.

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Learn when the GDPR may apply to your research, what you should do to be compliant, and where to go for further information.

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GDPR: Top Noncompliance Risks and Mitigation Strategies

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Identify activities that may pose a risk to GDPR compliance.

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FERPA: A Quick Review of the Law for Researchers and IRBs

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Learn about the Family Educational Rights and Privacy Act (FERPA) as it relates to and impacts research that uses student educa...

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FERPA and Online Learning in the Time of COVID-19

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This webinar covers student data privacy issues with online learning including compliance with FERPA and other regulations.

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Professional Development Webinars

IRB Administrator Professional Development and Self-Advocacy

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Learn how to grow and develop yourself as an IRB administrator.

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Research Administration Webinars

Tips for Research Administrators: Working with Faculty and Research Teams

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Provides research administrators with tips related to working with faculty and research teams.

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How to Effectively Manage a Research Administration Team

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Provides research administrators with strategies to build, improve, and retain employees.

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Research Focus Webinars

CRISPR Genome Editing: Rewriting DNA and the Future of Humanity

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Describes CRISPR genome editing, including its applications and ethical questions.

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Gender and Sexual Minorities (GSM) in Human Subjects Research

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Provides a review of GSM communities and important considerations when members participate in research.

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Higher Education Accelerated Credit

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Describes the differing forms of accelerated credit available to students and recognizes potential challenges within the post-s...

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Research in Wound Care

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Learn about one research team’s experience in conducting wound care research.

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Responsible Conduct of Research Webinars

From Cancer to COVID-19, Does Science Self-Correct?

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Discusses the effects of bad science, the history and role of retractions in research, and the impact of COVID-19 research.

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Importance of Peer Review and Data Validation in Research

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This webinar covers the types, limits, and ethical guidelines of peer review along with federal regulations and criteria for evaluating proposals.

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Revised Common Rule Webinars

Transitioning Research to the Revised Common Rule: The What, How, and Why

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Learn about considerations and challenges for transitioning pre-existing research to the revised Common Rule, as well as requir...

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Revised Common Rule: Overview of Revisions

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It has been more than six months since the revised Common Rule’s implementation date, revisit the revisions it made using thi...

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Revised Common Rule: Revisions to Informed Consent

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Explores the revised Common Rule’s updates to informed consent. Focuses on key changes, new elements, and updates to existing...

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Revised Common Rule: Revisions to Definitions

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In-depth review of revisions to the definitions section of the Common Rule. Covers new terms added, updates to existing definit...

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Technology Transfer Webinars

Intellectual Property and Working With Your Technology Transfer Office

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An in-depth review of intellectual property for faculty and researchers.

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Technology, Ethics, and Regulations Webinars

Successfully Developing and Deploying Digital Clinical Measures

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Provides an overview of successful remote monitoring across clinical research, clinical care, and public health.

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Privacy and Ethics for Connected and Automated Vehicles

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An overview of connected and automated vehicles (CAVs) and the associated privacy and ethical challenges.

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Facial Recognition Considerations for Researchers

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Covers the use of facial recognition systems in research and healthcare.

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FAQs

Are webinars available as part of an organizational subscription?

No, webinars are not part of an organizational subscription. However, organizations can subscribe to our All Access Webinar Package which includes all of CITI Program’s currently available webinar recordings as well as future recordings released during a subscription period*. Organizations can also subscribe to individual webinars or our Diversity Training in Clinical Research Webinar Package.
*This product includes most CITI Program generated webinars. Some webinars offered through special / partner programs may not be offered as part of this package.

Can I download the slides?

Yes, after you purchase the webinar recording, you will have access to the webinar’s contents including to the handout of the slides that can be used to follow along or take notes as you watch the recording.

I registered for a webinar, but was not able to attend. Can I access the recording for free?

If you were not able to attend the webinar, you may purchase the recording as an independent learner. Each individual webinar will have a "Buy Now" link on its catalog page.

How do I find out about future, live webinars?

CITI Program will send notification of upcoming webinar registrations to organizational administrators, previous webinar attendees, and all learners who have completed a related course in the previous year. If you would like to receive registration notifications, please contact us to be added to the webinar mailing list.

Do webinars provide any completion documentation?

Yes – webinars function as modules in our LMS. If learners have a webinar added to their gradebook, they will receive a completion report or certificate just as if they have completed a traditional CITI Program module.