Introduces the basics of planning for and managing data generated through SBE research involving human participants.

This course is intended to cover the core elements of HIPAA requirements as applicable for education and research roles.

Introduces R01s and provides key information for individuals seeking to write their first R01.

Covers key concepts in scholarly publishing and provides an overview of the publication process for both traditional and hybrid...

Considerations for sex and gender variables in research.

Addresses some of the dos and don’ts of engaging diverse populations in research.

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These guides provide resources and guidance for developing and facilitating in-person or virtual RCR training sessions.

Discusses ways that sponsors, sites, and clinical research organizations can transform the clinical trial experience.

Explores the role of predictive analytics in higher ed, its ethical challenges, and ways to implement it ethically.

Provides learners with practical tips to make ADA, Section 504, and accommodations in the 21st century more accessible and equi...

Reviews best practices and challenges for navigating collaborative research partnerships in a global environment.

Discusses strategies to address researcher noncompliance with IRB-approved protocols.

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Introduces healthcare professionals to the basic concepts and expectations of HIPAA.

Provides an overview of methods used to decontaminate laboratory materials.

Learn about QA/QI programs, how to conduct an internal audit, and strategies for using the findings.

Provides strategies and information pertinent to disaster response and research reactivation.

Meets the requirements of a general laser safety training program for research and medical institutions.

Provides an overview of the U.S. DOE’s interim policy on conflicts of interest.

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Covers covers the core principles of the 5S system and illustrates why using 5S is essential to a “Lean” initiative.

An in-depth review of the Clery Act and how higher education institutions can comply with applicable regulations.

Provides an overview of NIH Career Development (“K”) Awards.

Introduces regulations and their application as they relate to subrecipient monitoring.

Provides research administrators with strategies to build, improve, and retain employees.

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.

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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.

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.