Clinical Research Coordinator / Study Coordinator Training Program
The Clinical Research Coordinator (CRC) Training Program was developed in collaboration with some of the top coordinators from North America, extending across all types of practices and therapeutic areas. The comprehensive nature of this course brings together the expertise of many disciplines in the industry.
The CRC training program was designed for both clinical research coordinators who are entering the industry and those who are looking to develop their skills further. The program is offered in a module based format, from which students are able to pick those modules which are most relevant to their role. Please see the downloadable course syllabus below for a listing of modules and course content.
The program is offered in a custom built Learning Management System (LMS) which will track progress of each student and issue a certificate of training for all modules completed. This certificate and syllabus should be retained as evidence of training for sponsors, CROs, ethics boards and regulatory authorities.
This course is offered via an on-line, self-paced eLearning platform. The eLearning environment is custom built to cater to the three primary learning styles, in an engaging setting. Practical job aids are included which can be used by the student in their role as a Clinical Research Coordinator.
This course has been designed to provide comprehensive, performance based content blended with real world applications. After reviewing the comprehensive content, students will use scenario based learning to apply these skills and ensure retention of the content.
Comprehensive, foundational training of clinical research coordinators has been shown to:
The Clinical Research Coordinator training program will teach students to run a complete clinical trial from start to finish. The following modules are contained in this course:
- Introduction to Clinical Research & The Clinical Research Coordinator
- Good Clinical Practice
- Informed Consent
- Ethics Boards
- Study Protocols
- Site Trial Master File and Essential Documents
- Preparing for a Study / Study Start Up
- Conduct of a Study
- Data Management, Case Report Forms and Electronic Data Capture
- Safety Monitoring and Reporting
- Study Closure
- Study Monitoring
The estimated time to complete this course is 13 hours
The cost to purchase this course is $500
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