OVERVIEW

10-Week Clinical Research Associate (CRA) & Clinical Research Coordinator (CRC) Beginner Program is organized by Barnett International and will be held from Jan 16 - Mar 20, 2019. This CME Conference has been approved for a maximum of 30 hours (3.0 CEUs) of continuing education credit.

The target audience for this medical event is Aspiring Clinical Research Associates and Clinical Research Coordinators (This course is also appropriate for Clinical Research Associates and Clinical Research Coordinators with less than six months of experience), College Students and New Graduates in a Scientific Field, Nurses.

Conference Description:
The online 10-Week CRA & CRC Beginner Program provides a comprehensive introduction to clinical research and the job functions of the Clinical Research Associate (CRA) and Clinical Research Coordinator (CRC) for drug, biologic, and device trials. This program is geared toward individuals seeking a new career or career change into clinical research, but haven’t decided which job track to pursue. Case studies and industry best practices are presented to emphasize how the learning objectives apply directly to the responsibilities of the CRA and CRC.

The resources required to take this on-line course are already at your fingertips - an Internet connection and a phone. After registering, you will receive an email confirmation that provides you with the Web Seminar link and audio connection information.

Prior to the start of the course, participants will receive comprehensive course materials. Come to class prepared to interact – you will be able to ask questions, provide feedback and participate in discussions and group work. Upon course completion, participants will be provided training certificates. In order to receive accreditation CEUs, participants are required to pass both a mid-term and final exam. Upon completion of the exams, CEU certificates will be provided.

Conference Objectives:
• Describe and discuss the investigational product development process, including FDA regulations, ICH guidelines, and Good Clinical Practice (GCP)
• Explain the roles and responsibilities of a CRA and CRC
• Describe the four types of monitoring visits, including the responsibilities of the CRA and CRC in preparation, activities, and follow-up
• Explain the Key Pre-Study Concepts: Role of the Principal Investigator, Site Selection, Clinical Trial Agreement and Budget Negotiation

Additional details will be posted as soon as they are available.