The Collaborative Institutional Training Initiative (CITI Program) is dedicated to serving the training needs of colleges and universities, healthcare institutions, technology and research organizations, and governmental agencies, as they foster integrity and professional advancement of their learners.
These courses explore key topics related to research security and international engagement.
This series provides a comprehensive overview of cybersecurity in healthcare, exploring organizational strategies, technical defenses, and risk management practices to safeguard data, operations, and trust.
Equips research personnel with the skills and insights necessary for effective mentorship.
This course prepares researchers and educational technology developers to navigate COPPA’s legal requirements, conduct compliant research, and engage with digital environments used by children under 13.
Describes the regulatory framework and quality programs for HCT/Ps
This interactive course helps university students understand their Title IX rights and responsibilities, including how to recognize, prevent, and report sexual misconduct and discrimination.
This course offers advanced training for experienced researchers and leaders in responsible research conduct, emphasizing integrity, ethical leadership, and fostering healthy research environments.
This course equips community partners with the knowledge and skills to ethically and effectively engage in research.
This course provides essential practices for those working with high-risk biological materials, clarifying biosafety vs. biosecurity and enabling practical biosecurity planning to prevent theft, misuse, or intentional release.
This course equips faculty, staff, and administrators with the fundamentals and tools to measure outcomes, improve learning, and effectiveness.
The IRB Review of Exempt Research course provides an overview of the exempt categories of research per 45 CFR 46.104 and discusses considerations for making an exempt determination per regulatory criteria.
Examines the application of IRB exemptions, focusing on overlooked flexibilities in categories 1 through 3 through discussion and real-world examples.
Introduces you to key information about, and tools to use, the 3Rs of animal research.
The RCR Casebook course is a collection of real-world ethical dilemmas designed to promote discussion, critical thinking, and skill-building in RCR.
Covers the principles, governance approaches, practices, and tools for responsible artificial intelligence (AI) development and use.
Explores how behavioral science can enhance compliance programs.
Explores the transformative impact of AI on biomedical research, addressing its unique characteristics, potential to exacerbate health disparities, and the urgent need to redesign research processes and incentives to ensure ethical and equitable knowledge discovery.
Explores how generative AI (GenAI) can support science communication.
The webinar explores effective collaboration between IACUC and IBC, detailing their roles, regulatory responsibilities, and best practices to ensure safe and ethical life sciences research while enhancing oversight and protecting workers and animals.
Explores issues that lead to research misconduct and ways to develop trust with faculty and leadership.
This webinar for IRB, IACUC, and sponsored program administrators covers seven key compliance elements with strategies and case studies to strengthen research, reduce risk, and promote integrity.
Reviews two of the foundational elements of the Common Rule—when something is or is not research and when an individual is or is not a human subject.
Provides an in-depth review of the elements of informed consent.
A detailed review of the IRB meeting and membership requirements.
This course provides graduate students with practical guidance, strategies, and resources to confidently navigate each stage of the dissertation process from proposal to defense.
Provide your organization's learners with access to currently available and future webinar recordings.
An introductory video-based series to the NSF’s SBIR-STTR funding program and a discussion of key elements of the proposal and proposal process.
Presents a scalable model for creating a research coordinator float pool to provide flexible staffing, structured training, and broad support for clinical research across institutions.
Describes how to calculate the appropriate sample size for different study designs and outcomes.
Explores the benefits and the considerations of working with consultants on research misconduct investigations.
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.
A complete research compliance suite that supports IRB, IACUC Conflict of interest, Bio Safety Export Control, and more.
HRP Consulting provides customized services for your research program, including temporary staffing, IRB/IACUC assistance, accreditation support, program evaluations, training/education and more.
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.
CITI Program courses are approved for CME credits through the Albert Einstein Montefiore Continuing Professional Development Center (CPDC). Albert Einstein College of Medicine-Montefiore Medical Center (Einstein) is accredited by the Joint Accreditation for Interprofessional Continuing Education to provide continuing education activities for healthcare professionals. Einstein is accredited to offer continuing education credit for the following professions: medicine, nursing, psychology, pharmacy, dentistry, optometry, social work, nutritional science, and athletic training.
CITI Program is also accredited by the International Accreditors for Continuing Education and Training (IACET) and offers IACET CEUs for its learning events that comply with the ANSI/IACET Continuing Education and Training Standard. IACET is recognized internationally as a standard development organization and accrediting body that promotes quality of continuing education and training.
Highlighted below are just a few select subscribers & collaborators.
Our courses are built by over 350 highly qualified experts and rigorously peer reviewed to incorporate various perspectives and ensure accuracy, completeness, and overall quality.
Debra Thurley, JD, is an Assistant Vice President for Research at The Pennsylvania State University where she provides leadership and oversight to the University’s ten research compliance programs. Debra also serves as the Deputy Research Integrity Officer, overseeing the research misconduct process at the University.
Kimberly White has served as the Vice President, Corporate Privacy Officer at Northwell Health for nine years. She is an attorney by background, previously working as a commercial litigator, and earning her JD from Northwestern University and BA from New York University. She is also certified in healthcare compliance.
Clinton Schmidt oversees the Conflict of Interest and Commitment program at Penn State University, which is responsible for research-related COI, Institutional COI, and Conflicts of Commitment. Clint is also responsible for the institution’s Research Security Program, which helps researchers collaborate successfully while protecting against foreign influence.
Ms. Deyanira Santiago is currently, the Director of Science Administration and the Institutional Official at the Wistar Institute. She is responsible for the oversight of research compliance activities related to animal research, human subject protections, and occupational and biosafety, as well as institutional research resources.
English Language Arts Teacher
I liked how user-friendly the course modules were.
Adjunct Faculty
The methodology, presentation of the topics, and language used were very pleasant. You do not get bored or annoyed, because the development is very dynamic and understandable.
Graduate Student
Concise, informative, and interactive. Great job to the team that put this together!
Study Nurse
I liked that this course is offered in multiple learning styles (reading and video) and that you can stop and return to the content when needed.
New Course – Data Privacy 101
This course provides learners with a foundational understanding of why privacy awareness and compliance matter in today’s data-driven world.
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On Research Podcast – Opening Doors in STEM: Service Dogs, Advocacy, and Research Accessibility
Season 3 – Episode 13 – Opening Doors in STEM: Service Dogs, Advocacy, and Research Accessibility In this episode, we explore how service dogs and...
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Clinical Center Ethics Grand Rounds: Reducing Use of Animals in NIH Researc...
Join the NIH on February 4 for a presentation titled "Clinical Center Ethics Grand Rounds: Reducing Use of Animals in NIH Research."
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