CRC 3.0 Accredited Post-Graduate Certified Clinical Research Coordinator Program with 3 remote internships, Drugs and Medical devices

The CRC new course prepares you to work in the field of clinical research and leads to the certification as Clinical Research Professional. Our course is based in Good Clinical Practice with a focus on Canadian and American regulatory perspectives. The program includes both theoretical and practical elements.

Available on the online learning platform Moodle, the course includes 23 chapters including

• Introduction to clinical research
• The pharmaceutical industry
• Ethics and history of clinical research
• Clinical trial phases
• Good Clinical Practice: foundations and application
• Roles in clinical research
• The clinical trial protocol
• Case report forms
• Recruitment and retention
• FDA and US regulations
• The impact of Covid-19 on clinical trials
• Canadian and international regulations
• The role of the Ethics Board/IRB
• Informed consent
• Adverse event reporting
• Study design
• Essential documents in clinical research
• Site evaluation and selection
• Site initiation
• Monitoring visits
• Study close-out
• Fraud
• Data management
• Information privacy
• Electronic data capture
• Audits
• Data Safety Monitoring Boards

Beyond the theoretical foundations of clinical research, we provide:

• Remote internship tasks including with Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC)
• Clinical Trial Monitoring simulation activities
• Practical tasks based on real-life requirements and scenarios which provide hands-on experience
• 1:1 advising on CV and interviews
• Live help 7 days a week by email or Skype

The program is entirely online and self-paced. Most people take from 1 to 3 months to complete it.

The advantage of our program is that it provides the flexibility and cost-effectiveness of an online program, with access to live help 7 days per week.