To complete a refresher course, follow the instructions below:
Full Answer
CITI Program offers a variety of refresher courses so learners can meet retraining requirements with fresh content. Additional modules of interest within HSR allow for exploration of several important topics and may be selected to meet organizational needs.
The Refresher Training will take approximately 2 hours. Each DOE site IRB Administrator or Training Manager will work with CITI administrators to set up individual site requirements by site listing on the front page of the DOE CITI access page. How often do I need to take human subjects education?
After you log into CITI, you will be brought to your main menu. This will show any previous courses you have taken, as well as course status. To add a new course, select “Add a Course or Update Learner Groups.” 4. Scroll down towards the bottom of the page, and click “Continue to Question 1 at this time.”
After completing all the required modules and quizzes, CITI will automatically send a completion certificate to the DOE Site IRB Administrator who will then record the training requirement in the individual records. Others will be required to track their own training records. How long will it take to complete the course?
How do I take the CITI refresher courses? Log in to the CITI webpage. Once you log in you will see the link to the Student/Faculty Basic course in human subjects training. Once you proceed at that link CITI will automatically guide you through the required CITI refresher modules.
approximately 2 hoursHow long will it take to complete the course? Each CITI module has text to read and a quiz to complete. The average learner spends approximately 4.5 hrs in the Basic Course site and approximately 1.5 hours if your site requires additional modules. The Refresher Training will take approximately 2 hours.
An average score of 80% or higher is required in order to successfully complete a CITI training course. If I do not pass a module exam, can I retake it? Yes, the test modules may be taken as many times as needed. When you complete the test and do not pass, you can select Re-enter.
CITI training courses expire every 3 years and CITI will send e-mail reminders 90 days before your courses expire. The refresher courses are automatically added to your curriculum, and will be visible, when you log into your account.
The official answer is that you should take a refresher course every 12 months after your initial certification as your skillset degrades over time. It is the halfway point between your original certification and when you are required to renew so it's a pretty good rule to follow.
Do I need to take CITI training? Investigators and study personnel doing research involving human subjects must take CITI training before receiving IRB approval, and become re-certified at minimum every three years.
Allegations of inappropriate use will be investigated, and the results may be reported to the organization(s) with which a learner is affiliated. Inappropriate use may result in immediate account suspension or termination.
If you already have a CITI account, sign into your account and click on the course to complete the course, or select “Add a Course or Update Learner Groups” to add another course.
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.
You can register now to take CITI Program content assigned to you by your organization for no charge. If you need training not provided by your organization, you can register as an independent learner and purchase the content required.
How many modules are required? You will be required to take 4 - 6 basic modules depending on the Basic course you choose. If you wish, you can take additional optional modules. The Refresher courses require approximately 4 - 8 modules.
Describes the important issues relating to publishing research results and working with authors. It also discusses the potential pitfalls and errors that can lead to research misconduct and authorship disputes, as well as strategies for avoiding and resolving authorship disputes.
Discusses styles of collaboration and potential trade-offs relating to collaborative research. It also identifies some of the complexities of managing and assessing collaborations, and special considerations involved in collaborative work, including working with industry, across disciplinary and international boundaries, and with students.
Explains why conflicts of interest can be ethically problematic and how organizations can have a conflict of interest.
Discusses effective approaches to responsible data management and key issues related to data storage, sharing, and reporting.
Identifies the roles and responsibilities of mentors and those that they mentor. It also describes how to avoid research-related problems and optimize the mentoring experience, as well as barriers to mentoring, particularly for women and minority researchers, and potential solutions to these barriers.
Discusses the history and evolution of peer review, value of peer review as it relates to publications and grant awards, ethical issues associated with peer review, and ethical duties of a peer reviewer.
Discusses the definition of plagiarism, appropriate summarization of material, and strategies for properly citing information sources.
GCP ICH Refresher reinforces the importance of concepts covered in the basic level GCP for Clinical Trials with Investigational Drugs and Biologics (ICH Focus) course.
Provides a basic understanding of the ICH’s role and impact on conducting clinical research according to GCP. It describes the purpose of ICH and identifies the basic requirements for compliance with ICH GCP.
This course provides training that meets IATA and DOT packaging/shipping requirements.
No. GCP training is a separate training and is not basic human subjects protection training. GCP principles are specific to clinical trials and include international ethical and scientific quality standards for designing, conducting, recording, and reporting clinical trials.
The National Institutes of Health (NIH) in fulfillment of their GCP training policy (Policy on Good Clinical Practice Training for NIH Awardees Involved in NIH-funded Clinical Trials; NOT-OD-16-148) states that NIH-funded investigators and staff should be trained in GCP.
GCP content is suitable for research teams involved in clinical trials of drugs, biologics, and devices, as well as those involved in behavioral intervention and social science research studies.
GCP for Clinical Trials with Investigational Drugs and Medical Devices (U.S. FDA Focus) and GCP FDA Refresher are suitable for individuals proposing to conduct clinical trials of drugs and devices primarily in the U.S. and/or who would prefer a more U.S. FDA-centric curriculum.
GCP courses vary on the number of modules they contain. Modules consist of detailed content, images, supplemental materials (such as case studies), and a quiz. Learners may complete the modules at their own pace.
Yes, five of CITI Program's GCP courses are mutually recognized. See the individual course pages for more information on TransCelerate mutual recognition, including requirements (such as module requirements) for organizations and learners to utilize the mutually recognized courses.
Learners who fulfill a GCP course’s requirements (complete all the required modules after the effective date) will see a statement in the Description field on their Completion Report’s “Transcript Report” (part 2 of a Completion Report) or on their Certificate.
After logging in to CITI and finding the correct course, the course page displays only the basic course in lieu of the refresher course. If your training has been expired for an extended period of time, you may not be eligible to take the refresher course and should instead re-take the basic course.
CITI Refresher Course Instructions If your CITI training has already expired, you will see this screen upon logging into the system. Click either Group í or Group î _ depending on which course was completed previously. Although this looks like the original course, the modules will be labeled as a refresher once you click on the course.
If you fail to complete the required CITI HRP Refresher course you will receive an expiration notice. Failure to complete the required CITI training course will delay approval of IRB submissions and could jeopardize an individual's ability to engage in human subjects research. What should I do if I forget my login information?
The module also describes the stakeholders affected by reproducibility problems, a collection of reproducibility initiatives, and strategies that can mitigate or prevent irreproducibility. *Note, this module is part of the CITI Program's Responsible Conduct of Research (RCR) Basic course, but is also included in this course.
For Biomedical and Social Behavioral courses, CITI will automatically add the "Refresher" course to your list of courses 90 days before your CITI Training expires. To complete the Refresher course before this time or to recertify for the GCP course, please see instructions below*
The basic course expires two years after the month/date it was taken. For example, if you completed the course on Oct. 15, 2010, it expires on Oct. 16, 2012. You will need to take the CITI refresher course to keep your human research protections training current.