Clinical Research Coordinator / Study Coordinator Training Program

 

Advantage Clinical’ s Clinical Research Coordinator online training program is designed for both research coordinators who are entering the industry as well as those who are looking to develop their skills further.

The Clinical Research Coordinator (CRC) Training Program was developed in collaboration with a number 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 program is offered in a custom built online Learning Management System (LMS) which has been designed to optimize content delivery to our students, track / evaluate their progress and issue certificates of training. This certificate and syllabus should be retained as evidence of training for sponsors, CROs, ethics boards and regulatory authorities.

Practical job aids are included which we encourage students to use in their role as a Clinical Research Coordinator.

Our award winning instructional designers have designed the content of this course to provide comprehensive, performance based content blended with real world applications. After reviewing the comprehensive content, students 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:

  1. Introduction to Clinical Research & The Clinical Research Coordinator
  2. Good Clinical Practice
  3. Informed Consent
  4. Ethics Boards
  5. Study Protocols
  6. Site Trial Master File and Essential Documents
  7. Preparing for a Study / Study Start Up
  8. Conduct of a Study
  9. Data Management, Case Report Forms and Electronic Data Capture
  10. Safety Monitoring and Reporting
  11. Study Closure
  12. Study Monitoring
  13. Audits
  14. Quality Management in Clinical Research

Download the detailed course syllabus

The estimated time to complete this course is 12 hours

The cost to purchase this course is $625

 

All of our course offerings are covered by our Customer Satisfaction Guarantee. If you are not satisfied with your purchase we will provide a full refund.


Note that course purchases are mediated through PayPal and will require a credit card to complete the transaction.

Non-credit card purchases, and those including group discounts, will be processed manually. Please email sales@advantage-clinical.com to coordinate this type of purchase.

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Purchase a Course

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Group Licensing and Non-Credit-Card Purchases

For non-credit card and group/licensing purchases please email sales@advantage-clinical.com, or contact us through the web site.



Available Courses:

 Clinical Research Coordinator /
 Study Coordinator Training Program
 Good Clinical Practice Training (E6R2)  GCP E6 Release 2 Bridge Course  Patient Recruitment for Research Sites  Patient Recruitment for Sponsors  Introduction to Clinical Research  Clinical Trial Site Audit Preparedness
  Purchase This Course

In order to proceed with course purchase please register for an account. You will then be directed to the purchase functions. Upon purchase you will receive immediate access to the course content by logging into the site.