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Clinical Research Associate

Becoming a CRA (CRA001)


Description
This online 10-Week CRA Program provides a comprehensive
introduction to clinical research and the job functions of the Clinical Research
Associate (CRA) 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. Upon completion,
The online 10-Week CRA Beginner Program provides a comprehensive
introduction to clinical research and the job functions of the Clinical Research
Associate (CRA) 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. Upon completion,
The Axon Clinical Research Academy will provide resume assistance so that you can
position yourself for entry into this market.
Content
  • Module 00 - Introduction to the CRA Journey
  • Upload completed certificate
  • Module 1: Recommended introductory video.
  • Module 1: Introduction to Clinical Research and Clinical Trials
  • Module 1: Good Clinical Practice
  • Module 1: Clinical Research Roles and Responsibilities
  • Module 1: Commonly Used Abbreviations in Clinical Trials
  • Module 1: Take Quiz
  • Module 2: Study Design & Protocol
  • Module 2: Study Design & Protocol - The Exercise
  • Module 2: Study Design & Protocol - Sample Protocol
  • Module 2: Study Design & Protocol Exam
  • Module 3 : The Role of a CRA (Monitor) Part I
  • Module 3: The Role of A CRA (Monitor) Part II
  • Module 3.mp4
  • Module 3: Role of a CRA - Homework
  • Module 3: The Role of A CRA (Monitor) Exam
  • Module 4: ICH GCP and SOPS - A Monitor's Bible Part I
  • Module 4: ICH GCP and SOPS - A Monitor's Bible Part II
  • Module 4: ICH GCP and SOPS Exam
  • Module 5: Pre-Study Visit and Site Initiation Visit Part I
  • Module 5: Pre-Study Visit and Site Initiation Visit Part II
  • Module 5: Pre-Study and Site Initiation Visit Exam
  • Module 6: Interim Monitoring Visit and Close Out Visit Part I
  • Module 6: Interim Monitoring Visit and Close Out Visit Part II
  • Module 6: A Glimpse into the CRA role
  • Module 6: Interim Monitoring and Close Out Visit Exam
  • Module 7: Monitoring Activities - SDV - Part I
  • Module 7: Monitoring Activities - SDV - Part II
  • Module 7: Monitoring Activities - Source Data Verification - Source Docs
  • Module 7: Monitoring Activities - Source Data Verification - Protocol
  • Module 7: Monitoring Activities - Source Data Verification - Test Instructions
  • Module 8: Interview Preparation
  • Module 8: Resume Preparation and Mock Interview
  • Module 9: Prepare for Final Exam
  • Module 9: Prepare for Final Exam - Homework
  • Module 10: Final Exam and Exit
Completion rules
  • All units must be completed
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