Non-OSP Training
Training for Researchers and Research Administrators
Office of Clinical Trials Training
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Clinical Research Updates (PDF)
Provides the most recent updates pertaining to clinical trials at the University, which was presented at UNC’s NRP June Meeting. -
Clinical Research Personnel Training
This training provides guidance and an overview on working as a clinical research personnel at the University. -
Good Clinical Practice (GCP)
GCP is the international ethical and scientific standard expected in the design, conduct, performance, monitoring, auditing, recording, analysis, and reporting of clinical trials. Effective October 1, 2014, all UNC-CH investigators and research staff who are involved in the design, conduct, or reporting of clinical trials involving human subjects AND a drug, device, or biologic are expected to document completion of GCP training.
Conflict of Interest (COI) Training
COI Training is required for all individuals involved in research at UNC-Chapel Hill. The training will inform the individual of the University’s policies on conflict of interests, individual disclosure responsibilities and the Federal regulations on financial conflict of interests. Training must be reviewed and completed at least every four years.
Environmental Health and Safety (EHS) Training
EHS provides guidance and training on how to understand and comply with regulations regarding biological, chemical, radioactive and other hazardous material used in research.
Finance Training
Training and documentation provided by the UNC Finance Office for ConnectCarolina and related finance applications, such as InfoPorte and ePro.
Health Insurance Portability and Accountability Act (HIPPA) Training
Training for campus personnel regarding protected health information (PHI) and its transmission.
Institutional Animal Care and Use Committee (IACUC) Training
IACUC provides oversight of all animal subjects used in research at the University in compliance with Federal regulations.
Office of Human Research Ethics (OHRE) Training
Training provided for the ongoing educational process for Institutional Review Board (IRB) members, the staff of the IRB Office, campus researchers and their related administrative team on the ethical concerns and regulatory and organizational requirements for the protection of human subjects research.
- Collaborative Institutional Training Initiative (CITI)
All faculty and staff involved in Human Subject Research at the University must complete required CITI training related to the protection of human subject research.
Office of Research Information Systems (ORIS) Training Portal
This resource includes training from various central offices and centers involved in research at the University and provides a training tracking system for users.
Research Compliance Learning Community
A resource offered by the Research Compliance Program that includes training resources and contact information to aid campus researchers and department administrators involved in research at the University.
Responsible Conduct of Research (RCR) Training
A resource offered by the Research Compliance Program that includes the University’s Plan for Training in RCR along with helpful information for other research related resources.
- Center for Faculty Excellence Guide for RCR (PDF)
- NC TraCS RCR Training Schedule
- Office of Postdoctoral Affair’s RCR Training Schedule
NCURA Award Lifecycle Webinar
The NCURA Lifecycle of the Award webinar series offers training on several broad research administration topics relevant to research institutions. Start your training here .
External Training Resources
- National Council of University Research Administrators (NCURA) Education Opportunities
- National Institutes of Health (NIH) Grants Training
- National Institutes of Health (NIH) eRA Commons User Guides
- National Science Foundation (NSF) Toolkit
- Grants.gov User Help
- Society of Research Administrators International (SRAI) Education Opportunities