Learn strategies for promoting equity, diversity, and inclusivity in clinical research participation.

Discusses the importance of a QA program, how to develop a QA program, and the expected outcomes of a QA program.

Foundational course on how to develop, negotiate, and implement a clinical trial budget.

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.

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

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

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Covers the unique issues associated with big data and data science research ethics.

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

Understand factors that may determine participant payment decisions.

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.

This course provides learners with a review of contemporary bioethics issues.

This course covers the core norms, principles, regulations, and rules governing the practice of research.

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The synergistic relationship between best practices, regulations, and professional experience forms the foundation for working in a BSL-3 facility.

An introduction to the Family and Medical Leave Act (FMLA) in the context of higher education.

This course provides an introduction to federal fraud and abuse laws.

This course provides training on the elements contained in the ISO 14001 specification for Environmental Management Systems, and the benefits of implementing these elements.

These guides provide resources and guidance for developing and facilitating in-person or virtual RCR training sessions.

Provides learners with key information on the management of controlled substances in clinical research settings.

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This course addresses ways to create and maintain healthy workplace environments in various research settings.

Describes ways to overcome difficulties in study start-ups.

Provides effective approaches to negotiating clinical trial agreements.

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

Describes the process and considerations for publishing a scientific paper.

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

Browse all of the courses and series available from CITI Program.

CTrials helps grow sponsored research programs by taking on the many administrative challenges inherent in managing clinical trials.

Informed Consent Builder is a cloud-based platform that streamlines the process of managing and generating informed consent forms.

Protocol Builder is an online protocol writing and collaboration platform that also speed up your pre-review turnaround times.

N2 is a not-for-profit alliance of Canadian research networks and organizations working to enhance national clinical research capability and capacity.

BIC Study Foundation is a resource for those who want to take CITI Program courses in Korean. They are a certified training provider by the Korean FDA/MAFRA for HRPP and ACU Programs.