Training by Content Area

This training library links to relevant training from across all campus Units, as they pertain to specific processes.

Consult this training library to organize the catalogue by role.

I want to:

Trainings for international research:

Training Course	Audience	Learning Objectives	Time Duration	Contact
Export Compliance at a Glance	Recommended Program Managers, Department Chairs Required Researchers working with export-controlled projects	Conceptualize regulation of Export Controls Understand that how Export Compliance connects to both domestic and international research Navigate Export Compliance processes Know when to contact the Export Compliance Office	10 minutes	Export Compliance
Restricted Party Screening with Visual Compliance	Required Administrators who need access to Descartes Visual Compliance to manage financial, material or research transactions. Required Administrators who need access to Descartes Visual Compliance to support global exchange.	Conduct a restricted party screening in Visual Compliance. Contact Export Compliance for alert adjudication.	20 minutes	Export Compliance
Concur Training Basic Training Delegate and Approver Training Advanced Training Booking Travel	Required Travelers booking travel Required Delegates booking travel	Book travel in Concur Request and reconcile travel and event expenses	Varies	Travel Team
Global Travel Policies	Recommended Travelers	Book travel in Concur Request and reconcile travel and event expenses	1 hour	UNC Global

Trainings for research disclosure requirements:

Training Course	Audience	Learning Objectives	Time Duration	Contact
Conflict of Interest Training	Required All UNC Researchers	Navigate University COI policy Navigate research transparency measures	15-20 minutes	Conflict of Interest
In-person Responsible Conduct of Research Training RCR Webpage, Post-Doc Webpage	Required Anyone conducting UNC Research must take either In-Person or Modular Responsible Conduct of Research Training Required All NIH Researchers must take in-person training Recommended All post-docs, regardless of funding source, are encouraged to select the in-person training. Non-NIH Post-Docs can satisfy UNC training requirements with the appropriate CITI Modules	Conduct research with integrity Avoid fabrication, falsification, and plagiarism in research	Offered each semester	Eric Everrett, Research Integrity Officer
Modular Responsible Conduct of Research	Required Anyone conducting UNC Research must take either In-Person or Modular Responsible Conduct of Research Training Required All NIH Researchers must take in-person training Recommended All post-docs, regardless of funding source, are encouraged to select the in-person training. Non-NIH Post-Docs can satisfy UNC training requirements with the appropriate CITI Modules	Conduct research with integrity Avoid fabrication, falsification, and plagiarism in research	9-10 modules	Eric Everrett, Research Integrity Officer

Trainings for research with human participants:

Training Course	Audience	Learning Objectives	Time Duration	Contact
Biomedical Research: Citi Training for Human Subjects Research Group 1, Biomedical Research	Required for: Biomedical Research: Medical, physiological or pharmacological studies that typically involve direct contact with subjects. Includes, but is not limited to, research with drugs, devices or other interventions. Renew every three years	Conduct medical, physiological, or pharmacological studies that involve direct contact with patients	10-20 minutes per module, 2-3 hours total	OHRE/IRB
Social and Behavioral Research Research: Responsible Conduct of Research Training Group 2, Social and Behavioral Research	Required for: Social and Behavioral Research: Studies on sociological, psychological, anthropological or educational phenomena that typically involve direct contact with subjects. Does not include drug or device studies. Renew every three years	Conduct research on sociological, psychological, anthropological, or educational phenomena involving direct contact with subjects. Does not include drug or device studies	10-20 minutes per module, 2-3 hours total	OHRE/IRB
Data and Specimens ONLY: Citi Training for Human Subjects Research Group 3, Data and Specimens ONLY	Required for: Research with Data and Specimens ONLY: No direct contact with human subjec Renew every three years	Conduct research with records, data, or biological samples. No direct contact with human subjects.	10-20 minutes per module, 2-3 hours total	OHRE/IRB
Citi Training for Human Subjects Research Good Clinical Practice (GCP) Training	Required for: All investigators and research staff involved in the design, conduct or reporting of clinical trials involving human subjects. Renew every five years	Apply the practices of Good Clinical Practice to clinical research	10-20 minutes per module, 2-3 hours total	OHRE/IRB

View the Office of Human Research Ethics’ required training webpage and training and resources webpage for further information and training opportunities.

Trainings for research with animal subjects:

Training Course	Audience	Learning Objectives	Time Duration	Contact
Laboratory Animal Coordinator Lecture	Required Researchers working with animal subjects	Overview IACUC, OACU protocol process Review Laboratory Animal Coordinator Responsibilities Manage inspections	10 minutes
Mouse Case Density Lecture	Required Researchers working with animal subjects	Understand University Policy on for mouse cage management	10 minutes
Animal Care Application Process (Offered Quarterly)	Recommended Researchers working with animal subjects	Review animal care application process	30 minutes
Inspections 101	Recommended, offered by request Researchers working with animal subjects	Apply animal care best practices to the laboratory Prepare for inspections	30 minutes
Division of Comparative Medicine Rodent Management Trainings	Required Researchers working with animal subjects	Maintain appropriate records for animal research	10 minutes

Visit the IACUC Training Webpage for further information.

Trainings for managing data concerns:

Training Course	Audience	Learning Objectives	Time Duration	Contact
Citi Training for Human Subjects Research	Good Clinical Practice (GCP) Training: All investigators and research staff involved in the design, conduct or reporting of clinical trials involving human subjects. Renew every five years	Navigate University COI policy Navigate research transparency measures	-

Questions about training? Contact our training manager.

Training by Content Area

I want to:

Conduct international research

Review disclosure requirements to participate in research

Conduct research with human participants

Conduct research with animal subjects

Manage Data Privacy and Data Retention Concerns