+1 (514) 534-0273, +1 (514) 257-3003 info@cra-school.com

Accelerated Access Clinical Research Professional Course (only for GCP-trained and experienced professionals)

$890.00

The Clinical Research Professional Accelerated-Access Course includes 3 remote internships in Canadian/US regulatory environment, but provides no diploma, as exams are not required. The course content is available for reference purposes only and a Letter of reference is provided to highlight the activities done during the internships.

Only for already GCP-trained professionals, who need only some practical “hands-on” experience to get eligible for interviews.

Unlimited Placement Assistance Till Hired (PATH) program is also included, providing students with all the tools to find and obtain employment within this industry: Networking coaching, CV adaptation support for every vacancy, interview practice and preparation for every role, professional branding and positioning, etc

N.B.: This program is only for GCP-trained/experienced professionals: Before registering online, please contact us at info@cra-school.com to verify your eligibility and discuss a suitable Action Plan that fits best your qualification and objectives.

Before enrolling, you can take online this basic GCP test to assess your GCP knowledge and your eligibility.

Description

Our CRP Accelerated Access Course is designed for GCP-trained professionals. Our Placement Assistance Til Hired (PATH) program is also included, providing students with the tools to find and obtain employment within this industry. Also included:

  • Internship tasks, to demonstrate essential clinical research experience
  • Monitoring modules
  • Access to a Clinical Trial Management System (Datatrak)
  • Pitch On Air interview simulator

This course has no tests or assignments, and does not result in a diploma.

Please contact us to ensure that you are eligible, before registering online! 

This course covers the following topics:

  • US Regulations and the FDA
  • Canadian and International Regulations  Ethics Review Boards
  • Informed Consent
  • Adverse Events
  • Study Design
  • Essential Documents
  • Site Evaluation and Selection
  • Site Initiation
  • Monitoring Visits
  • Study Close-Out
  • Fraud
  • Data Management
  • Information Privacy
  • Electronic Data
  • Audits
  • Data and Safety Monitoring Board
  • Medical Devices

 

N.B.: This program is only for GCP-trained/experienced professionals.
Email a request for admission to info@cra-school.com

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