Watch and Learn: Educational Modules
The UB CTSI’s Watch and Learn educational module videos are designed to increase the knowledge and performance of clinical researchers at UB and its affiliated institutions in order to help in the development of a large, diverse, and well-trained workforce of investigators and research teams. These brief videos, ranging from 5 to 30 minutes, offer an overview and/or practical guidance on a wide variety of research-related topics ranging from study development to dissemination of research results.
STUDY DEVELOPMENT
Topics relevant to the phase in which researchers are preparing their project (e.g., conceptual considerations, feasibility assessment, document development).
The studio model features direct input from participating stakeholders to better inform research design and dissemination.
Aug. 9, 2023
See how plain language can help researchers better connect with the communities they serve and develop stronger interdisciplinary science.
May 30, 2023
Understand Investigational Device Exemption (IDE) studies and the key role these play in medical device development.
Apr. 13, 2022
What is the NIH Public Access Policy, and how is it applicable to University at Buffalo investigators? Discover how to comply and learn answers to frequently asked questions.
Feb. 10, 2022
Learn whether your research study requires registration on ClinicalTrials.gov, as well as the consequences of not registering a study on the site.
Oct. 19, 2021
STUDY SUBMISSION
Topics relevant to the phase in which researchers are preparing to submit their project for approval (or activation) (e.g., application process, submission of study-related documents, review of regulatory and administrative processes).
Researchers need to understand their responsibilities when using the UBIRB as IRB for multi-site research.
Dec. 19, 2024
Learn the ins and outs of using an external IRB, including researcher responsibilities, requirements from the reviewing IRB, and steps taken by the UB IRB and reviewing IRB.
Aug. 9, 2024
Explore informed consent as well as the differences between a waiver and alterations of consent, when each is appropriate, and how to request these from the IRB.
Apr. 23, 2024
Discover what defines informed consent, where to find the consent form template, and how to best deliver information to potential subjects.
Dec. 14, 2023
Learn how Human Subjects Research is defined, what constitutes Exempt Human Subjects Research, and how to proceed.
Sep. 5, 2023
Learn how and why the Central Study Registration system was established, as well as the advantages of registering your study.
May 4, 2022
Explore the procedures you need to follow, how to ask for help, and what needs to be done in order to complete and finalize your clinical trial budget.
Oct. 21, 2021
Learn about the work that Clinical Research Facilitators do during the pre-review step of the human subjects research approval process at UB.
Oct. 6, 2022
Understand the types of review, steps, and typical timelines a new human research study may undergo after it has been determined that IRB review is required.
Feb. 16, 2022
STUDY EXECUTION
Topics relevant to conducting a clinical research study (e.g., implementation, trial management, participant and data safety and quality monitoring).
Learn how OnCore, a comprehensive management system, manages the life cycle of a research project and enhances the process of clinical research.
Oct. 19, 2021
Learn how to register your study and gain a better understanding of how to use ClinicalTrials.gov Protocol Registration and Results System (PRS) in this step-by-step guide.
Jan. 31, 2022
Learn why and how you need to enter the results of your clinical trial in the ClinicalTrials.gov Protocol Registration and Results System (PRS).
Mar. 29, 2022
Discover how the CTSI helps investigators troubleshoot recruitment and retention issues from the grant planning stage all the way through active recruitment.
Sept. 29, 2022
STUDY TOOLS AND RESOURCES
A variety of useful tools and resources for researchers (e.g., research 101, recruitment resources, dissemination).
Learn how Click automates the submission, review, and approval processes while managing all major administrative aspects of the research and compliance lifecycle.
Apr. 12, 2024
See how REDCap helps investigators create and design projects by offering a vast array of tools that can be tailored to virtually any data collection strategy.
Apr. 27, 2023
Discover how i2b2 and TriNetX, two de-identified clinical patient databases available to UB investigators, can serve as useful recruitment resources.
Jan. 4, 2023
Discover the modules in the Click Portal, how they support a study from project development through the approval process, and how to register for training.
Oct. 19, 2021
A series of short videos created by UB’s Office of Research Advancement for faculty planning to apply for funding opportunities.
Feb. 3, 2022
Looking for additional educational resources? Click here to learn more about upcoming CTSI Open Research Office Zoom sessions or to watch past sessions.
Ready to take a deeper dive into research principles and ethics? Check out the CTSI Core Competency Workshop Series focusing on Good Clinical Practice and Responsible Conduct of Research. Workshop recordings are available upon request; contact cmp9@bufflo.edu for access.