This course is designed to give hands-on practical experience to those new in the field who hold little clinical research knowledge, experience or skills. At the end of this course, the employee will receive a certificate for the course.
Course content:
- The History, Structure and Functions of Clinical Research
- Data Management, ICH-GCP Regulations and Review Boards
- Study Participant Management (Informed Consent & Safety), Privacy of Information and Quality Control (Monitoring)
- Essential Document Maintenance in compliance with Canadian and International Regulations and Quality Assurance (Audit & Inspection)
Training is conducted onsite, over a 3-day period equaling 21-hours, accommodating a maximum of 3 persons.
Offered in English and in French.
