Webinars

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

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.

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

Explores various types of noncompliance and their impact.

Examines ethical and policy issues about xenotransplantation.

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

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

Reviews public health duties, resources challenges, workforce response, and collaborating with regional hospitals.

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

The webinar details the functions of clinical data managers in the production of clinical trial results.

Sponsor-patient engagement yields more ethical and clinically relevant research.

Describes ways to overcome difficulties in study start-ups.

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

Provides effective approaches to negotiating clinical trial agreements.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Explores current challenges and improvement strategies related to informed consent.

Presents remote consent considerations and scenarios.

Explore informed consent issues with wearable tech research.

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

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

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

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

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

Explores considerations for a human research protection program (HRPP) emergency preparedness plan.

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

A systematic approach to exploring the barriers, steps, methods, and solutions for including service dog handlers in science.

A basic systematic approach is used to understand and apply federal regulations as they relate to service dogs.

A systematic approach to preparing for and adjusting to risks associated with wilderness field research.

An infection control introduction for researchers.

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.

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

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.

After the rigor of completing funding applications, this webinar discusses various tactics for success post-award.

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

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

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

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

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

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

A review of allowability of expenditures on federally supported projects.

Understand CUI and the obligations it creates for universities and researchers.

A general overview of FMLA and special considerations for grant-funded research.

A look at the challenges international students face in the U.S. and advice on how to help students navigate their journey.

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

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

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

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

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

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

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

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

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.

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

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

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

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

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

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

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

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

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

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

An introduction to blockchains and their potential for higher education.

Reviews FCPA as it relates to university research.

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

Explore the concepts of studying up, studying down, and studying sideways.

Explores ethical and regulatory considerations for human subjects research in outer space.

Explores what is known about IRB utilization of outsize expertise.

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

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

Considerations for sex and gender variables in research.

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

Understand factors that may determine participant payment decisions.

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

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

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

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

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

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

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

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

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

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

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

Discusses social media use in research recruiting.

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

Strategies to work with your reviewing IRB.

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

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

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

Reviews DoD requirements and limitations for research.

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

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

Learn about what to expect when participating in vaccine research.

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

Identify activities that may pose a risk to GDPR compliance.

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

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

Introduces core concepts of supervision and the supervisory process.

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

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

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

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

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

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

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

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

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

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

Explores the role institutions can play in supporting ethical authorship practices and resolving authorship disputes.

Examines mentorship in biomedical and behavioral research, which is critical to advancing science.

Learn how grant stewardship obligations are a part of responsible conduct of research.

Describes the process and considerations for publishing a scientific paper.

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

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

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

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.

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.

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

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

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

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

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

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

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

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

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

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.

Covers how to identify red flags in your survey data, strategies to develop surveys to minimize fraud, and best practices for data management.

Explores strategies for remaining diligent about securing online survey research.

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.

Explores the importance of ethics for AI companies and its impact on public trust and profitability.

Explores robots in healthcare and their ethical issues.

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

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

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

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