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Webinars

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

Organizations

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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 (CRCs), 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

Handling of Hazards in Research Animal Facilities

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Covers the types of hazards in research animal facilities, risk assessment of hazards, hazard mitigation, and the role of oversight committees and other research professionals.

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Conducting a Literature Search for Animal Use Alternatives

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Learn about the 3Rs, where to find 3Rs resources, and how to conduct a literature search for animal use alternatives in a database.

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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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Reviews public health duties, resources challenges, workforce response, and 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

Study Start-Up: Challenges and Strategies

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Describes ways to overcome difficulties in study start-ups.

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Infection Control/Prevention and Pandemics

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A review of infection prevention, lessons learned, and preparing for future pathogens.

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Managing Risk by Contract

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Provides effective approaches to negotiating clinical trial agreements.

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CRA Relationships with CRCs

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Details ways to produce productive partnerships between clinical research associates and clinical research coordinators.

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CRAs and Interim Monitoring Visits

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Discusses the process and content of a CRA’s interim monitoring visit.

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From Protocol to Manual of Procedures (MOP)

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Discusses the usefulness of a manual of procedures as a supplement to a clinical trial protocol.

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Discrete Choice Experiments with Neurologic Disorders

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Discusses discrete choice experiments, including their design, analysis, and ethical considerations.

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Clinical Trial Staff Diversity and Cultural Humility

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Discusses how clinical trial staff diversity and cultural humility can yield diverse subject recruitment and improved study outcomes.

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Understanding ISO 14155:2020 Revisions

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This webinar examines the new ISO 14155 medical device standard while exploring its implications for sponsors and investigators.

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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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Conflicts of Interest Webinars

U.S. Department of Energy Interim Policy on Conflicts of Interest

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Provides an overview of the U.S. DOE’s interim policy on conflicts of interest.

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Disaster Planning and Response Webinars

Disaster Response and Research Reactivation Efforts

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Examines ways to improve future disaster response and research reactivation approaches.

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Environmental Health & Safety Webinars

What Researchers Need to Know about Infection Prevention

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An infection control introduction for researchers.

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Sustainable Science: How to Make Research Labs Greener

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Discusses the environmental impact of research in the U.S., how to mitigate the environmental impact of research operations, and ways to involve key stakeholders in mitigating the environmental impact of research operations.

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Building a Laser Safety Program

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Provides key information on starting and maintaining a laser safety program.

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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

Writing Your First R01

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Introduces R01s and provides key information for individuals seeking to write their first R01.

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New Data Sharing Requirements for NIH-Funded Research

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Overviews the NIH Data Management and Sharing Policy’s scope and requirements.

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NIH Career Development (“K”) Awards - Matching Needs to Opportunities

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Provides an overview of NIH Career Development (“K”) Awards.

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Successfully Navigating Subrecipient Monitoring

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Introduces regulations and their application as they relate to subrecipient monitoring.

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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

Universal Design in Online Course Design

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Universal design principles and real-life examples are presented in this webinar.

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Design With the End in Mind

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The basics of backward instructional design are covered during this webinar.

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Artificial Intelligence: The Impact on Academic and Research Integrity

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AI is always evolving and this webinar will go over the (current) basics of artificial intelligence in relation to academic and research integrity.

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Burnout and Wellbeing in U.S. Higher Education

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This webinar looks at sources of burnout in higher education, national datasets, and recommendations for increasing employee wellbeing.

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Mentoring Learners and New Faculty Engaged in the Doctoral Quest

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Explores the relationship between learners and mentors and ways to develop an effective relationship.

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AI in Higher Education: An Overview

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Explores the role of predictive analytics in higher ed, its ethical challenges, and ways to implement it ethically.

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Effectively Communicating Research Results to Non-Scientific Audiences

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Learn how to communicate research results to the public and policymakers using different models and strategies.

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Title IX: 50 Years and Modern Challenges

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An in-depth review of the historical impact of Title IX and how to navigate modern challenges within higher education to ensure compliance.

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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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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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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

Utilizing Outside Experts on the IRB

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Explores what is known about IRB utilization of outsize expertise.

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In This Together: Meaningful Community Engagement in Research

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Addresses some of the dos and don’ts of engaging diverse populations in research.

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Advance Research Directives

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Discusses how advanced directives can be used in research and shares available resources.

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Why Sex Matters from Research to Patient Care

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Considerations for sex and gender variables in research.

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NIH Data Management and Sharing Policy for SBER: Implications for Researchers and IRBs

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Learn about the NIH Data Management and Sharing Policy’s impact on SBER.

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Paying Participants in Research: Regulations, Ethics, and Practical Considerations

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Understand factors that may determine participant payment decisions.

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How to Conduct an Audit of a Ceded Study

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QA/QI professionals can learn to audit ceded studies for single IRB (sIRB) review.

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Quality Improvement Activities and the Common Rule

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Learn to differentiate between QI activities and the types of activities that constitute regulated research involving human subjects.

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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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Explores aspects of virtual IRB meetings including the benefits, tech setup, documentation, and more particularly 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

Supervision for Supervisors

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Introduces core concepts of supervision and the supervisory process.

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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

Process Improvement and Research Administration

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Describes how to apply the Lean Six Sigma principles to research administration process improvements.

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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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Research Security Webinars

NSPM 33 Research Security Programs Standard Requirement Draft

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Provides an overview of the draft NSPM 33 Research Security Programs Standard Requirement and key considerations.

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Responsible Conduct of Research Webinars

The Process of Publishing a Scientific Paper

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Describes the process and considerations for publishing a scientific paper.

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Facilitating Synchronous RCR Training Sessions

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Describes facilitated discussions on the responsible and ethical conduct of research, including effective strategies for facilitation, participation, and productive discussions.

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The Dilemma Game App: How to Facilitate a Discussion on Research Integrity

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Explains how to facilitate an open discussion on research integrity using the Dilemma Game App.

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Peer Review Fundamentals

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Covers the purpose, best practices, and emerging models for peer review.

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NSF Plagiarism Investigations and Strategies to Prevent Plagiarism

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This webinar discusses a multi-year study on research misconduct completed by the NSF’s Office of Inspector General and how researchers utilize strategies to avoid plagiarism.

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Promoting Statistical Rigor in Scientific Manuscripts

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Provides practical advice on issues that often arise during statistical reviews of scientific manuscripts and explains the most common pitfalls and how to avoid them.

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Introduction to Meta-Analyses

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Provides a general overview of the methods and analytic techniques used in meta-analyses.

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Changing Security Requirements from U.S. Federal Research Funding Agencies

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Reviews NSPM-33, disclosure expectations, and the role of ORCID as digital persistent identifier.

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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

Healthcare Robot Ethics

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Explores robots in healthcare and their ethical issues.

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Drones in Academia

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Explores the use of drones in research and the regulations and requirements researchers and administrators need to know.

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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.

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_gat_UA-33803854-7	1 minute	This is a pattern type cookie set by Google Analytics, where the pattern element on the name contains the unique identity number of the account or website it relates to. It appears to be a variation of the _gat cookie which is used to limit the amount of data recorded by Google on high traffic volume websites.
_gcl_au	3 months	This cookie is used by Google Analytics to understand user interaction with the website.
_gid	1 day	This cookie is installed by Google Analytics. The cookie is used to store information of how visitors use a website and helps in creating an analytics report of how the website is doing. The data collected including the number visitors, the source where they have come from, and the pages visted in an anonymous form.
_hjAbsoluteSessionInProgress	30 minutes	No description available.
_hjFirstSeen	30 minutes	This is set by Hotjar to identify a new user’s first session. It stores a true/false value, indicating whether this was the first time Hotjar saw this user. It is used by Recording filters to identify new user sessions.
_hjid	1 year	This cookie is set by Hotjar. This cookie is set when the customer first lands on a page with the Hotjar script. It is used to persist the random user ID, unique to that site on the browser. This ensures that behavior in subsequent visits to the same site will be attributed to the same user ID.
_hjIncludedInPageviewSample	2 minutes	No description available.
_hjIncludedInSessionSample	2 minutes	No description available.
_hjTLDTest	session	No description available.
_uetsid	1 day	This cookies are used to collect analytical information about how visitors use the website. This information is used to compile report and improve site.
BrowserId	1 year	This cookie is used for registering a unique ID that identifies the type of browser. It helps in identifying the visitor device on their revisit.
CFID	session	This cookie is set by Adobe ColdFusion applications. This cookie is used to identify the client. It is a sequential client identifier, used in conjunction with the cookie "CFTOKEN".
CFTOKEN	session	This cookie is set by Adobe ColdFusion applications. This cookie is used to identify the client. It provides a random-number client security token.
CONSENT	16 years 5 months 4 days 4 hours	These cookies are set via embedded youtube-videos. They register anonymous statistical data on for example how many times the video is displayed and what settings are used for playback.No sensitive data is collected unless you log in to your google account, in that case your choices are linked with your account, for example if you click “like” on a video.
vuid	2 years	This domain of this cookie is owned by Vimeo. This cookie is used by vimeo to collect tracking information. It sets a unique ID to embed videos to the website.

Advertisement cookies are used to provide visitors with relevant ads and marketing campaigns. These cookies track visitors across websites and collect information to provide customized ads.

Cookie	Duration	Description
bscookie	2 years	This cookie is a browser ID cookie set by Linked share Buttons and ad tags.
IDE	1 year 24 days	Used by Google DoubleClick and stores information about how the user uses the website and any other advertisement before visiting the website. This is used to present users with ads that are relevant to them according to the user profile.
MUID	1 year 24 days	Used by Microsoft as a unique identifier. The cookie is set by embedded Microsoft scripts. The purpose of this cookie is to synchronize the ID across many different Microsoft domains to enable user tracking.
test_cookie	15 minutes	This cookie is set by doubleclick.net. The purpose of the cookie is to determine if the user's browser supports cookies.
VISITOR_INFO1_LIVE	5 months 27 days	This cookie is set by Youtube. Used to track the information of the embedded YouTube videos on a website.
YSC	session	This cookies is set by Youtube and is used to track the views of embedded videos.
yt-remote-connected-devices	never	These cookies are set via embedded youtube-videos.
yt-remote-device-id	never	These cookies are set via embedded youtube-videos.

Others

Other uncategorized cookies are those that are being analyzed and have not been classified into a category as yet.

Cookie	Duration	Description
_app_session	1 month	No description available.
_gfpc	session	No description available.
_uetvid	1 year 24 days	No description available.
_zm_chtaid	2 hours	No description available.
_zm_csp_script_nonce	session	No description available.
_zm_cta	1 day	No description
_zm_ctaid	2 hours	No description available.
_zm_currency	1 day	No description available.
_zm_mtk_guid	2 years	No description available.
_zm_page_auth	session	No description available.
_zm_sa_si_none	session	No description
_zm_ssid	session	No description available.
AnalyticsSyncHistory	1 month	No description
BNI_persistence	4 hours	No description available.
BrowserId_sec	1 year	No description available.
CookieConsentPolicy	1 year	No description
cred		No description available.
f	never	No description available.
L-veVQq	1 day	No description
li_gc	2 years	No description
owner_token	1 day	No description available.
PP-veVQq	1 hour	No description
renderCtx	session	This cookie is used for tracking community context state.
RL-veVQq	1 day	No description
twine_session	1 month	No description available.
UserMatchHistory	1 month	Linkedin - Used to track visitors on multiple websites, in order to present relevant advertisement based on the visitor's preferences.
web_zak	past	No description
wULrMv6t		No description
zm_aid	past	No description
zm_haid	past	No description