Preparing CRA, CRC & CDM Professionals for Clinical Research since 1989
The CRA Training Institute

The CRA Training Institute


Online CRA, CRC & CDM Clinical Research Courses

Get Trained and Certified for exciting careers in Clinical Trials Monitoring Globally

Receive your Certificate and be job-ready in as little as 3-4 Weeks!

The CRA Training Institute

At The CRA Training Institute our Accredited Online Clinical Research Courses are designed for persons with or without prior on-site clinical trials experience, seeking qualifications and/or current practical knowledge to effectively work as a Principal Investigator (PI), Clinical Research Associate (CRA), Clinical Research Coordinator (CRC), Clinical Data Coordinator or Clinical Data Manager (CDM) in the monitoring of clinical trials globally in all countries that follow the ICH-GCP guidelines for conducting clinical trials.  Many CROs and Pharma companies use our programs as CRA OnBoarding Training for new hires to their Clinical Research Jobs.

Clinical Trials in a Nutshell

Training Goals:

The goals of our online Clinical Research Associate training are to:

  1. To provide a thorough review of the good clinical practices (GCP), ICH, FDA/TPD regulations, roles, and responsibilities of the Clinical Research Associate/Monitor (CRA), Clinical Research Coordinator (CRC) or Clinical Data Manager (CDM).

  2. To provide graduates with the key skills, job criteria and industry expectations for the positions of Clinical Research Associate/Monitor (CRA), Clinical Research Coordinator (CRC) or...more
Clinical Research Associate Training

Simulation Exercises:

Students will participate in many online simulation exercises during the training program that will expose you to actual monitoring situations such as Investigator Selection, IRB Approval, CRF Review, SDV, Good Clinical Practice and Drug Accountability and Adverse Event assessment...more.


Training Objectives:

Upon completion of each course, participants will be able to:

  • Analyze and evaluate clinical data, to ensure investigator and site compliance with the study drug protocol, overall clinical objectives, FDA regulations, ICH Guidelines, Good Clinical Practice...more

Target Groups:

  • Nurses, Clinical Research Coordinators, Clinical Research Associates
  • Physicians, Dentists, Physician Assistants, Medical Monitors, Statisticians
  • Pharmacists, Pharmacologists, Database specialists, Principal Investigators
  • Medical Technologists, Laboratory Technicians, Pharmacy Technicians, Biostatisticians
  • Physical Therapists, Respiratory Therapists, Psychologists, Sociologists
  • Biologists, Chemists, Medical Writers, Clinical Data Managers.
  • Microbiologists, Biochemists, QC Analysts, 
  • and other life-science professionals.