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.
Provides instructions for creating the structures, personnel, and funding for a clinical research program.
Provides essential training on why privacy awareness and compliance matter.
A comprehensive introduction to ethical principles, regulations, and responsible practices that guide software and technology professionals throughout the software development lifecycle.
The course explores OPSEC in academia, training faculty, staff, and students to identify and mitigate risks to sensitive research data while upholding open science principles.
Equips university faculty, staff, administrators, and students with essential knowledge on Title IX compliance and program assessment to foster safer, more effective, and student-centered campus environments.
Helps clinical and operations leaders in safety-net and low-resource healthcare settings develop literacy and confidence in AI.
Equips research personnel with the skills and insights necessary for effective mentorship.
Explores how generative AI (GenAI) can support science communication.
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.
These courses explore key topics related to research security and international engagement.
Examines the application of IRB exemptions, focusing on overlooked flexibilities in categories 1 through 3 through discussion and real-world examples.
Provides a review of what COI committee members need to know.
Introduces you to key information about, and tools to use, the 3Rs of animal research.
This course provides learners with a review of contemporary bioethics issues.
The RCR Casebook course is a collection of real-world ethical dilemmas designed to promote discussion, critical thinking, and skill-building in RCR.
Explore the impact of academic integrity from the perspective of both students and faculty/staff.
Prepares you to apply digital health ethics in healthcare and research.
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.
Foundational and advanced courses provide critical information and best practices for IRB administration.
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 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.
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.
An overview of PCTs, their ethical complexities, best practices, and institutional considerations.
Provides the fundamentals of ergonomics across different settings.
Helps develop leadership skills to meet today’s changing, diverse, and dynamic environments.
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 faculty, staff, and administrators with the fundamentals and tools to measure outcomes, improve learning, and effectiveness.
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.
Kathryn Watkins is a research administrator with over 30 years of experience in university research management and administration. Kathryn is the owner and principal of K Watkins Research Administration Services, LLC, which provides hands-on assistance and educational content to institutions of higher education, small businesses, and non-profit organizations.
Marie has over 15 years of experience in quality, training, product compliance, and specifically controlled documents relating to FDA regulations and ISO standards. She has a Bachelor of Science in Healthcare Management and is currently the Document Control Specialist for Cadence Florida.
Blanca Flor Guillén-Woods, Partner at SLP4i, has implemented several applied research and evaluation projects, including multi-site and multi-year projects working with disenfranchised communities. Her experience includes research design, fieldwork, public opinion polling, conducting focus groups, facilitating community meetings, and quantitative and qualitative data analyses.
Tonya Ferraro is the Senior IRB QI Consultant at Boston Children’s Hospital’s (BCH) Education and Quality Improvement Program. Her responsibilities include educational outreach, internal reviews/audits, and supporting BCH’s reaccreditation effort. She holds a BA from Northeastern University and an interdisciplinary MEd from the University of Vermont focusing on research methodologies.
Postdoctoral Associate
I thought that the videos dramatizing various possible scenarios added a great deal to the written material. I also appreciated the inclusion of references to relevant philosophical and historical scholarship on research and methodological ethics.
PhD Student
The availability of two different platforms to deliver the information – written and audio-visual – catering to different learning styles was helpful. I also appreciated the self-paced modules that allowed you to return to complete unfinished work.
Postdoctoral Researcher
I really enjoyed the collaborative environment and the opportunity to learn from experienced colleagues. The sessions were well-organized, and I appreciated the practical examples that helped me understand complex concepts more easily.
Undergraduate Research Assistant
The infographics helped a lot with summarizing the overall concepts and main points.
New Course – Research Ethics for All (RE4All)
An accessible online course designed for community research partners with developmental disabilities who collaborate on social and behavioral research.
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NIH Seeks Public Comment on New Draft Resources for Implantable Device Trials
What Researchers, Sponsors, and Institutions Should Know In March 2026, the National Institutes of Health (NIH) released two draft resources to improve the design, conduct,...
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Science Based Non-Academic Careers (SNAC) Workshop – From NIH to Gene...
Join the NIH for the "From NIH to Genentech and Beyond: Navigating Careers in Pharma, Biotech, and the Startup Frontier" workshop on April 1.
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