Clinical Research Coordinator Roles and Responsibilities Training

Course Description This foundational course prepares clinical research coordinators (CRCs) with the essential knowledge and skills needed to navigate their roles and responsibilities across all phases of a clinical trial in accordance with Good Clinical Practice (GCP) guidelines. Participants will gain a thorough understanding of the clinical research team structure, human subject protections, informed consent, investigational product management, and the documentation and safety reporting requirements critical to trial integrity. By the end of the course, coordinators will be equipped to support regulatory compliance, engage effectively with IRBs and sponsors, maintain accurate trial records, and confidently approach audits and inspections. Learning Objectives Describe Investigator and coordinator responsibilities during the course of a clinical trial and apply GCP compliance Discuss mandatory critical interactions with Institutional Review Boards (IRBs) or Ethics Committees (ECs) Recognize critical elements of human subject protection Discuss the requirements for investigational product management and maintenance of adequate and accurate records for research trials Recognize key requirements for patient safety management and regulatory reporting. Discuss good documentation practices for clinical research trials Examine audit and inspection readiness Who Should Attend New and Aspiring Clinical Research Coordinators Clinical Principal Investigators Clinical Trial Assistants, Specialists and other Team Members Supporting Sites Instructor Nikki Christison, B.S., C.C.R.A.,T.I.A.C.R. Click here for complete trainer biographies Registration Fees $1,195* *Includes up to 20 participants per login at a single location. All participants (up to 20) are eligible for "Certificates of Attendance," and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional logins for other locations, please call +1 215.413.2471 or toll-free in the U.S. 800.856.2556, or email customer.service@barnettinternational.com for pricing. Accreditation Information Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 6 hours (0.6 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation. Barnett International will issue a receipt of completion for earned CEUs within three weeks of program completion. ACPE#: 0778-0000-23-025-L99-P. Released: 3/23. Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.