Title: Clinical Research Coordinator Roles and Responsibilities Training

Date: May 19 and 26

Time: 9:30am-12:30pm ET

• Introduction to Clinical Research, Investigational Product and Device Development, Regulatory Oversight and apply Good Clinical Practice Guidelines
• The Clinical Research Team: Roles & Responsibilities – PI, CRCs, IRBs, and Sponsors
• Protection of Human Subjects: Informed Consent Process and Considerations
• Essential Documents and Product Accountability
• Source Documentation, Safety Reporting, and Case-Report Forms
• Audits and Inspections

Advanced Registration Required

Note: This workshop will take place via 2 Webinar Sessions. Please note the dates and times of the zoom sessions below (Must attend both):

Webinar Session 1 - Tuesday, May 19, 9:30AM-12:30PM

Webinar Session 2 - Tuesday, May 26, 9:30AM-12:30PM