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 learners with practical tools for retaining research participants.
This course provides essential techniques to effectively gather valuable insights through focus group interviews.
Provides information on how to adopt and integrate telehealth or telemedicine technologies used to care for patients hospitalized with a highly infectious pathogen.
This role-based course provides the practical know-how to monitor clinical research sites effectively.
Take a deep dive into social media research, including ethical issues to consider during the research lifecycle.
Foundational overview of clinical research meant to prepare medical residents and fellows to conduct their own research and work on research teams.
Details the operational requirements for clinical research laboratories.
An in-depth review of advanced topics important to research administrators.
Introduces you to key information about, and tools to use, the 3Rs of animal research.
Covers the essentials of statistical analysis to help learners gain greater statistical literacy.
Introduces the basics of planning for, managing, sharing, and archiving data generated through biomedical research involving human participants.
Covers the unique issues associated with big data and data science research ethics.
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.
Explores robots in healthcare and their ethical issues.
Learn how grant stewardship obligations are a part of responsible conduct of research.
Explores the importance of ethics for AI companies and its impact on public trust and profitability.
Explores ethical and regulatory considerations for human subjects research in outer space.
AI is always evolving and this webinar will go over the (current) basics of artificial intelligence in relation to academic and research integrity.
Describes Quality Control’s role in helping a study adhere to protocol and regulatory guidelines.
Provides learners with the skills needed to create and manage controlled documents.
Learn about fraud, waste, and abuse (FWA) and ways to prevent and report FWA.
Provides learners with best practices for creating and maintaining study documents.
A role-based course that provides practical know-how to effectively lead or participate on data monitoring committees.
Empower yourself to effectively intervene and support others in critical situations with our comprehensive Bystander Training course.
Learn the operational considerations of implementing a telehealth service at your healthcare organization.
This course covers lean manufacturing as a production process based on an ideology of maximizing productivity while simultaneously minimizing waste within a manufacturing operation.
Stress at research institutions is common, explore ways to navigate and mitigate the effects of stress in these settings.
Explores strategies for remaining diligent about securing online survey research.
A basic systematic approach is used to understand and apply federal regulations as they relate to service dogs.
This webinar looks at sources of burnout in higher education, national datasets, and recommendations for increasing employee wellbeing.
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.
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.
Dr. Sullivan has been certified as a family nurse practitioner by the American Nurses Credentialing Center for the past 20 years and is an advanced practice nurse with prescriptive privileges. Dr. Sullivan’s clinical interest includes supporting students' complex and diverse health and mental health concerns.
Dr. Nancy Devino is Director of Sponsored Programs at the University of Texas Medical Branch at Galveston (UTMB). She holds a PhD in chemistry and served as a faculty member at two-year and four-year colleges before transitioning into full-time research development and administration.
Mr. Koopman provides business development and strategic advisory services to universities, investors, and life science startups. He has served as an officer and board member in several early-stage companies, as well as Director of New Ventures at NYU. He also spent more than decade in the investment banking and pharmaceutical industries.
Constance is an experienced import and export compliance professional. With 10+ years of experience as a regulatory compliance professional, Constance is a skilled practitioner in the areas of commodity classifications, transportation of dangerous goods and compliance auditing.
Clinical Research Nurse
I appreciate being able to learn via a recorded live presentation supported by slides containing key information. I like how the information can be saved and referenced at a later time.
Graduate Student
The modules were very thorough, easy to follow, and understand.
Assistant Professor & Postdoctoral Research Fellow
These courses were easy to access and succinct, which made a review of the Belmont Report key tenets, as well as the review of differences between practice and research, a focused and time efficient endeavor.
Professor
The course touches on important research considerations in a manageable format. The material required that I pay attention but did not tax my concentration.
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.
New Course – HIPAA and HITECH for Business Associates
This course provides a regulatory background, legal obligations, and best practices related to the HIPAA HITECH Act of 2009.
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