About the clinical research coordinator (CRC) course via CITI
Course title: | Clinical Research Coordinator (CRC) – Ba ... |
Course platform: | CITI |
Renewal Required: | Not at this time |
Target audience: | The CRC course is intended for CRCs, inv ... |
Required CRC module topics: | Clinical research coordinator overview P ... |
Full Answer
Clinical Research: An Introduction serves as a helpful precursor to taking CITI Program courses in the Good Clinical Practice (GCP) series, Human Subjects Research (HSR) series, and Responsible Conduct of Research (RCR) series. By providing a description of the conduct and context of clinical trials, this course provides leaners with the opportunity to better understand …
CRC courses provide foundational and advanced role-based training for clinical research professionals. The courses cover information that expands beyond but is directly connected to the Human Subjects Research (HSR) and Good Clinical Practice (GCP) courses.
The Trusted Standard in Research, Ethics, Compliance, and Safety Training. 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.
This course provides the basic concepts of what clinical research is, how it is carried out and by whom, and its underlying ethical and regulatory framework. It discusses the key principles of Good Clinical Practice such as data management and the protection of human subjects. It further explores specific issues in clinical research, including ...
Various Clinical Research Courses in IndiaS.No.CourseDuration1Post Graduate Diploma in Clinical Research1 year2Bachelor of Science in Clinical Research3 years3Master of Science in Clinical Research2 year4Certificate in Clinical Research6 monthsJul 19, 2021
GCP consists of basic and refresher courses that provide essential good clinical practice training for research teams involved in clinical trials. Improve site activation time and reduce training time with mutually-recognized, effective, engaging training.
The Collaborative Institutional Training Initiative (CITI) is a collaboration between the University of Miami and the Fred Hutchinson Cancer Research Center to develop a web based training program in human research subjects protections.
bachelor's of scienceMost entry-level clinical research associate positions require candidates to have a bachelor's of science (BS) in a health-related field from an accredited four-year university. In some cases, programs are designed to add practical hours needed to qualify for certification tests.
To receive a certificate, all quizzes must be completed with at least 80% accuracy. Upon successful completion of all quizzes, the user will be given access to the Certificate of Completion. Based on CTN Policies and Procedures, GCP certification expires after three years.
GCP training should be updated at least every 2 years.Sep 28, 2020
The cost to attend CITI Program – Collaborative Institutional Training Initiative ranges from $30 to $600 depending on the qualification, with a median cost of $100.Mar 24, 2021
The CITI Program is a subscription service providing free research ethics education to all members of our on campus research community. The CITI course is a protected site. If you are new to the site, you may gain access at the following link: https://www.citiprogram.org/?pageID=668.
To register for the CITI course, click Register for the CITI Course. You will then be asked to choose your institution. Individuals from Hunter College should choose Participating Institutions from the drop down menu, and then choose City University of New York (CUNY). Click Submit.
Clinical research is an attractive industry for researchers in India because it foresees enormous growth and job opportunities not only for trained medical, pharmaceutical, and paramedical professionals but also for project management staff, regulatory authorities, government, and the society at large.Jan 31, 2020
Pharmacovigilance (PV, or PhV), also known as drug safety, is the pharmaceutical science relating to the collection, detection, assessment, monitoring, and prevention of adverse effects with pharmaceutical products.
Protocol Builder is an online protocol writing and collaboration platform that also speed up your pre-review turnaround times. 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.
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.
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.
The CRC Advanced course provides clinical research professionals with advanced training tailored to the CRC’s critical role in the conduct of clinical trials. It is designed for CRCs who have taken CRC Foundations, or those with two or more years of experience as a CRC.
Provides an overview of project management principles, how the principles can be applied to managing clinical trials, and how using project management methodologies can increase trial efficiency by minimizing omissions and redundant activities. This module also discusses tools that CRCs can use to help manage a clinical trial.