A foundational course for individuals considering a career as a clinical research associate (CRA). The course provides broad training on the ethical, regulatory, and practical aspects of monitoring a research site. The modules explain how recent developments in clinical trial organization and conduct have changed the role of CRAs. In addition, the course details the communication and relationships among CRAs, sponsors, contract research organizations (CROs), clinical research coordinators (CRCs), and principal investigators.
Suggested Audiences: Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), Contract Research Organizations (CROs), Faculty, Principal Investigators (PIs), Research Administrators, Sponsors, Students
Author(s):
- Jessica Rosenbluth, MS - Syneos Health
- Natasha Williams, BSc - Narra Consulting LLC
- Robert Michalik, JD, RAC - RegulatoryPro Consulting
- Chinonso Singleton, MS - LIBRE, LLC
- Clareece West, BSc - West-Fenn Enterprise, LLC
To learn more about this course please visit: about.citiprogram.org/courses...
Негізгі бет CITI Program Course Preview - Clinical Research Associate (CRA)
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