The GCP – Social and Behavioral Research Best Practices for Clinical Research course introduces GCP principles and discusses how they apply to clinical trials using behavioral interventions and social science research. This course is presented in a dynamic, nine-module format with narration, interactive features, and downloadable resources.
It covers key topics in clinical research:
- Research Protocol
- Recruitment and Retention
- Informed Consent Communication
- Confidentiality and Privacy
- Participant Safety and Adverse Event Reporting
- Quality Control and Assurance
- Research Misconduct
The National Institutes of Health’s (NIH) “Policy on Good Clinical Practice Training for NIH Awardees Involved in NIH-funded Clinical Trials” establishes the expectation that all NIH-funded investigators and staff who are involved in the conduct, oversight, or management of clinical trials should be trained in GCP. This course helps behavioral and social science researchers meet that expectation.
The development of the GCP – Social and Behavioral Research Best Practices for Clinical Research course was supported by the National Center for Advancing Translational Sciences (NCATS), National Institutes of Health (NIH), through the Clinical and Translational Science Awards (CTSA) Program, grant number 3UL1TR000433.
Language Availability: English
Suggested Audiences: Clinical Research Coordinators, Contract Research Organizations (CROs), Investigators, IRB Members, Key Study Personnel, Principal Investigators, Research Nurses, Research Staff, Researchers, Sponsors, Study Coordinators
Organizational Subscription Price: Included in Good Clinical Practice (GCP) series for $1,000 per year/per site
Independent Learner Price: N/A