Webinars

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


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


Access to All Webinars

All Access Webinar Package (Organizations Only)
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Provide your organization's learners with access to currently available and future webinar recordings.

Webinars


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.

icon of computer display with overlapping documents
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

Research and Clinical Ethics Considerations for Xenotransplantation
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Examines ethical and policy issues about xenotransplantation.

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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.

CRISPR gene modifications DNA strand
COVID-19: Ethical Care and Workforce Concerns
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Reviews public health duties, resources challenges, workforce response, and collaborating with regional hospitals.

Webinars
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.

diverse fingerprints forming a tree


Clinical Research and GCP Webinars

The Role of Data Managers in Clinical Trials
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The webinar details the functions of clinical data managers in the production of clinical trial results.

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Sponsor-Patient Engagement: How Patients Shape Clinical Development
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Sponsor-patient engagement yields more ethical and clinically relevant research.

puzzle pieces representing engagement
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.

Icon with syringe, pills, and viral material
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.

individual hands holding each end of a plug
CRAs and Interim Monitoring Visits
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Discusses the process and content of a CRA’s interim monitoring visit.

file cabinet coming out of laptop display
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.

graphic of a laptop with pages from a manual flipping
Discrete Choice Experiments with Neurologic Disorders
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Discusses discrete choice experiments, including their design, analysis, and ethical considerations.

brain image with each section in a different bright color
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.

tablet with medical data next to a stethoscope
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.

hands presenting for a handshake inside a speech bubble
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.

Magnifying glass on on keyboard
Research Equity and the Part We Play
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Discusses ways to improve diversity and equity among clinical trial participants.

multicolored hands raised to show diversity
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.

icon of a stethoscope and clipboard with checkmarks
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.

Doctor and Woman discussing consent
Remote Informed Consent: The Same, but Different, but Still the Same
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Presents remote consent considerations and scenarios.

3D rendering of a computer monitor with a checkmarked document
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.

various windows with remote work employees
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.

Arrow going right through maze


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.

closeup insurance claim form on a clipboard


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

Emergency Preparedness and Response for HRPPs
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Explores considerations for a human research protection program (HRPP) emergency preparedness plan.

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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

Service Dogs in Science: Barriers to Inclusion
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A systematic approach to exploring the barriers, steps, methods, and solutions for including service dog handlers in science.

samson the service dog in the lab
Service Dog 101: Everything You Need to Know
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A basic systematic approach is used to understand and apply federal regulations as they relate to service dogs.

white service dog
Field Research Safety: Assessing and Managing Risk
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A systematic approach to preparing for and adjusting to risks associated with wilderness field research.

zoologist writing down data
What Researchers Need to Know about Infection Prevention
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An infection control introduction for researchers.

illustration of healthcare sanitation team
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.

icon of a beaker with green liquid and 2 leaves coming out of the top
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.

globe concept for export compliance


Grants Webinars

I’ve Been Funded, Now What?
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After the rigor of completing funding applications, this webinar discusses various tactics for success post-award.

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

graphic of a clipboard with check-marked items and a dartboard with a bullseye
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.

business people working together towards a goal
Successfully Navigating Subrecipient Monitoring
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Introduces regulations and their application as they relate to subrecipient monitoring.

hand holding a checkmark icon
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.

two people working at a table
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

Controlled Unclassified Information
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Understand CUI and the obligations it creates for universities and researchers.

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FMLA Essentials: Guidance for Employers in Grant-Funded Research Settings
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A general overview of FMLA and special considerations for grant-funded research.

young couple holding baby in front of calendar
Navigating the Mental Health of International Students
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A look at the challenges international students face in the U.S. and advice on how to help students navigate their journey.

two foreign students
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.

gear movement with arrows for direction
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.

brain with tech wireframe
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.

illustration of someone explaining data
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.

puzzle pieces representing compliance
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...

disabled group of people interacting
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.

globe where each hemisphere is a puzzle piece
Blockchain and Higher Education
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An introduction to blockchains and their potential for higher education.

squares in the shape of a circl representing blockchain
FCPA and University Research: What Faculty and Administrators Need to Know
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Reviews FCPA as it relates to university research.

Almost complete mirrored globe made of puzzle pieces
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

Studying Up, Studying Down, and Studying Sideways
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Explore the concepts of studying up, studying down, and studying sideways.

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Space Exploration: The Future of Human Subject Research Ethics
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Explores ethical and regulatory considerations for human subjects research in outer space.

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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.

diverse fists raised in unity
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.

illustration of a group of diverse men an women
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.

2 women coming out of their displays and sharing a folder
Paying Participants in Research: Regulations, Ethics, and Practical Considerations
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Understand factors that may determine participant payment decisions.

illustration of hands raised for questions
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 ...

Native American eagle feather
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.

Virtual Meeting on Laptop with multi-colored avatar icons
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.

3d green translucent medical marijuana cross
Understanding Consent Requirements and “Key Information”
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Explore the informed consent requirements related to increasing understandability and “Key Information."

glasses on top of consent documents
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.

3d globe made of social media and app tiles
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.

checkmark on a smart phone screen for informed consent and research protections
Working with Your IRB
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Strategies to work with your reviewing IRB.

Working With Your Irb Card
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.

illustration of two people with torso-sized puzzle pieces
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.

Military helicopter
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.

computer screen with combination lock and wheel protecting data
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...

child student raising hand for privacy
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.

Webinars


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.

Line traveling up steps symbolizing improvement


Research Administration Webinars

Successfully Navigating Stress in Research Institutions
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Stress at research institutions is common, explore ways to navigate and mitigate the effects of stress in these settings.

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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.

Illustration of a group of colleagues talking at conference table
How to Effectively Manage a Research Administration Team
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Provides research administrators with strategies to build, improve, and retain employees.

illustration of a group of diverse people


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.

rna enzyme complex
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.

LGBTQ+ Flag
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...

robed students throwing graduation hats in air
Research in Wound Care
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Learn about one research team’s experience in conducting wound care research.

Gauze and scissors for wound care


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.

graphic of woman on virtual interface with security shield behind it


Responsible Conduct of Research Webinars

Promoting Healthy Authorship Dynamics in Research Teams
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Explores the role institutions can play in supporting ethical authorship practices and resolving authorship disputes.

Digital book with education icons surrounding it
The Importance of Mentorship in Biomedical and Behavioral Research
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Examines mentorship in biomedical and behavioral research, which is critical to advancing science.

back to back heads with arrows and plant growth upward
RCR and Grant Stewardship
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Learn how grant stewardship obligations are a part of responsible conduct of research.

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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.

illustration of a group celebrating an idea
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.

icon of a head processing info with tablet in the foreground
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.

Icon of a lock intertwined with circuits
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.

Equal sign signifying reproducibility of research


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...

calendar showing common rule compliance date
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...

one following another meaning revision


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

Survey Research Fraud: Understanding Malicious Intent
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Explores common motives behind fraudulent survey research participation, how to address and mitigate the impact of identified fraudulent data, and how to minimize opportunities for malicious intent.

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Survey Research Fraud: Managing Your Data
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Covers how to identify red flags in your survey data, strategies to develop surveys to minimize fraud, and best practices for data management.

man at computer with checkmark on display
At Risk Survey Research Design: Remaining Diligent
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Explores strategies for remaining diligent about securing online survey research.

smart phone with security icon
Emerging Technologies and Homeland Security
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Explores the challenges and opportunities emerging technologies present to homeland security, covering topics such as cyber threats, ransomware, drone misuse, IoT vulnerabilities, AI threats, disinformation, and deepfakes.

us map depicted in digital nodes
Why AI Companies Should Care About Ethics
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Explores the importance of ethics for AI companies and its impact on public trust and profitability.

icon of a balance inside a computer chip
Healthcare Robot Ethics
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Explores robots in healthcare and their ethical issues.

extended robot hand
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.

Hovering drone with camera
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.

Smartwatches with health data
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.

illustration of car with connected electrical patterns
Facial Recognition Considerations for Researchers
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Covers the use of facial recognition systems in research and healthcare.

graphic of phone scanning face for recognition


FAQs

Are webinars available as part of an organizational subscription?

Yes, organizations can subscribe to our All Access Webinar Package as part of our custom Make Your Own base subscription option. The All Access Webinar Package includes all of CITI Program’s currently available webinar recordings as well as future recordings released during a subscription period*.

*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.