Take a deep dive into social media research, including ethical issues to consider during the research lifecycle.
This role-based course provides the practical know-how to monitor clinical research sites effectively.
Foundational overview of clinical research meant to prepare medical residents and fellows to conduct their own research and work on research teams.
This course covers lean manufacturing as a production process based on an ideology of maximizing productivity while simultaneously minimizing waste within a manufacturing operation.
A role-based course that provides practical know-how to effectively lead or participate on data monitoring committees.
A basic systematic approach is used to understand and apply federal regulations as they relate to service dogs.
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Provides information on risks and threats to the global research ecosystem — and the knowledge and tools necessary to protect against these risks.
Learn strategies for promoting equity, diversity, and inclusivity in clinical research participation.
This course introduces survey research design, implementation, analysis, and ethical considerations.
A systematic approach to preparing for and adjusting to risks associated with wilderness field research.
AI is always evolving and this webinar will go over the (current) basics of artificial intelligence in relation to academic and research integrity.
Examines mentorship in biomedical and behavioral research, which is critical to advancing science.
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Covers the principles, governance approaches, practices, and tools for responsible artificial intelligence (AI) development and use.
This course provides foundational training on conflicts of interest for healthcare professionals.
Describes facilitated discussions on the responsible and ethical conduct of research, including effective strategies for facilitation, participation, and productive discussions.
Explains how to facilitate an open discussion on research integrity using the Dilemma Game App.
Explores robots in healthcare and their ethical issues.
This course provides learners with a review of contemporary bioethics issues.
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An introduction to the Family and Medical Leave Act (FMLA) in the context of higher education.
This course teaches a systematic approach to investigating quality issues, creating effective corrective action plans rooted in...
This advanced, role-based course provides second-level training tackling topics of importance for experienced IRB administrators and HRPP directors.
This course provides necessary insight to understand, distinguish, and perform the spirit of the law as described in ADA of 1990 and 2003 and other relevant laws for compliance purposes.
Discusses the importance of a QA program, how to develop a QA program, and the expected outcomes of a QA program.
Meets the requirements of a general laser safety training program for research and medical institutions.
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Helps develop leadership skills to meet today’s changing, diverse, and dynamic environments.
Details ways to produce productive partnerships between clinical research associates and clinical research coordinators.
Discusses the importance of CRA soft skills in building productive relationships with sites and sponsors.
Covers the purpose, best practices, and emerging models for peer review.
Provides instruction on how to improve your teaching and training skills in a variety of settings.
Provides an overview of conflict, types of conflict, conflict styles, communication styles, and intervention strategies.
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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.
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