Clinical Research Fundamentals

This conference is presented two times per year. The content will enhance the understanding of the role and responsibilities of the clinical research coordinator by providing foundational knowledge. Attendees will acquire the tools necessary to improve performance of safe, ethical and compliant clinical research in the academic and clinical setting.

Go to Confluence to access slides (Jefferson campus key and password. log in required).

Below are the topics presented.

  • Identify and Locate Your Resources
  • Good Clinical Documentation
  • Adverse Events, Unanticipated Problems, and Safety Reporting
  • Monitor Visits and Audit Readiness
  • Informed Consent Process
  • Clinical Trial Billing and Epic
  • Investigational Product Management
  • Certification and Developing Quality

*Updated July 22nd, 2021