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.
Introduces the basics of planning for and managing data generated through SBE research involving human participants.
Covers covers the core principles of the 5S system and illustrates why using 5S is essential to a “Lean” initiative.
Foundational course on how to develop, negotiate, and implement a clinical trial budget.
Introduces R01s and provides key information for individuals seeking to write their first R01.
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.
Browse all of the courses and series available from CITI Program.
Foundational course covering the essential components of medical monitoring.
Strategies for implementing compliance with GDP, as well as standards and procedures for accurately completing Records required for current cGMP.
Describes FDA’s regulatory controls for common marketing approval pathways for the classes of medical devices, and explains the Code of Federal Regulations that pertain to medical device approval in the U.S.
Covers key concepts in scholarly publishing and provides an overview of the publication process for both traditional and hybrid...
Learn about the NIH Data Management and Sharing Policy’s impact on SBER.
Learn to differentiate between QI activities and the types of activities that constitute regulated research involving human subjects.
Browse all of the courses and series available from CITI Program.
These guides provide resources and guidance for developing and facilitating in-person or virtual RCR training sessions.
Explores the concept of race in clinical research and important ethical and regulatory questions.
Discusses ways to improve diversity and equity among clinical trial participants.
Understand factors that may determine participant payment decisions.
Discusses why technology-based expertise is critical to human subject protections and how to add IT insights to IRB review.
An overview of connected and automated vehicles (CAVs) and the associated privacy and ethical challenges.
Browse all of the courses and series available from CITI Program.
Learn about QA/QI programs, how to conduct an internal audit, and strategies for using the findings.
Reviews how to properly conduct an accident investigation, including identifying the root cause and implementing corrective act...
Describes regulatory requirements for a CAPA system in the biotech industry.
Provides an overview of the U.S. DOE’s interim policy on conflicts of interest.
QA/QI professionals can learn to audit ceded studies for single IRB (sIRB) review.
This course covers the fundamental safety practices for working with hazardous chemicals in the laboratory.
Browse all of the courses and series available from CITI Program.
Provides best practices for instructors on how to navigate the current challenges of online and hybrid learning while actively engaging with learners throughout the entire educational process.
Helps develop leadership skills to meet today’s changing, diverse, and dynamic environments.
Discusses the importance of CRA soft skills in building productive relationships with sites and sponsors.
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.
Provides learners with practical tips to make ADA, Section 504, and accommodations in the 21st century more accessible and equi...
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.
Tech Software a leading provider of SaaS compliance solutions for higher-education, academic medical centers, hospitals, government and biotech companies.
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.
Highlighted below are just a few select subscribers & collaborators.
Our courses are built by over 150 highly qualified experts and rigorously peer reviewed to incorporate various perspectives and ensure accuracy, completeness, and overall quality.
Sarah Ketchen Lipson is an assistant professor at the Boston University School of Public Health and Principal Investigator of the Healthy Minds Network. Her research focuses on understanding and addressing mental health in higher education and has been funded the National Institute of Mental Health, WT Grant Foundation, among others.
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.
PhD Candidate
The course was very informative and detailed. I also appreciated the case studies to assist in understanding how these concepts are applicable.
Clinical Nurse Specialist and Instructor
Very user-friendly
English Language Arts Teacher
I liked how user-friendly the course modules were.
Medical Doctor, Health Coach
I liked how the material was posted with big words, spaced, and simple English. The adverse drug event and monitoring sections were very informative.
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.
New Course – Data Management for SBE Research
The course provides insights on both practical and ethical issues related to managing data generated through human subjects research and uses examples to explain and illustrate core concepts.
Read the articleOn Campus Podcast – Graduate Student Advising
Season 1 – Episode 38 – Graduate Student Advising Advising at the graduate and doctoral levels at many institutions differs from advising at the undergraduate...
Read the articleFree Live Webinar – Why Sex Matters from Research to Patient Care
In this webinar we will differentiate the concepts of sex and gender and consider the impact of these variables on research outcomes and patient care.
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