We provide online Site Personnel Training and Sponsor Personnel (CRA/CRO) Training for Clinical Research

Site Personnel Training Program

Site Personnel

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Individual Enrollment
Group Enrollment

If you are an Investigator, Study Coordinator, or Pharmacist, enroll in this training program.

This program consists of core and advanced topics pertaining to GCP applicable to Clinical Research from the perspective of Investigational site.

This program is intended to provide the necessary training in the regulations and standards governing clinical trials in human subjects.

Our Site Personnel Training Program will provide you with a better understanding of your responsibilities in planning and conducting clinical trials.

Sponsor Personnel (CRA) Training Program

Sponsor/CRO Personnel

To view Course List and to enroll, click button:

Individual Enrollment
Group Enrollment

This program is intended for aspiring clinical research professionals as well as those who are already in the field. This includes personnel such as Clinical Research Associates (CRAs), Monitors and Project Managers at sponsor companies in the Biopharmaceutical industry, Contract Research Organizations (CROs) and other vendors.

This program includes courses that provide comprehensive training on topics related to Good Clinical Practice (GCP) applicable to clinical research from the Sponsor/CRO perspective.

Completion of this course enables you to learn the regulations and standards pertaining to clinical trials in human subjects and a better understanding of your roles and responsibilities in planning and conducting clinical trials.