The NextGen Clinical Trial Investigator Training is a virtual five-session educational program designed for investigators who currently lead or would like to lead clinical trials. The series includes lectures and panel discussions from leaders across the University of Missouri System, as well as Washington University, to define the regulatory, operational and ethical components of clinical trials, with the goal of developing a skilled workforce that provides the highest level of patient safety, teamwork and data quality. The program also covers institution-specific resources for investigators.

Timeframe: Five weeks, starting April 5 through May 3

• 5-6:30 p.m. - session program
• Additional videos to view to complete coursework

Follow the links below for speaker information at each session.

April 5 - Session 1: What is a Clinical Trial & Patient Perspective
April 12 - Session 2: Audit Ready Trials & Lessons Learned
April 19 - Session 3: Patient Recruitment & Informed Consent
April 26 - Session 4: Responsible Conduct of Research & Organizing Your Study Team
May 3 - Session 5: Institutional Resources

Session 5: Institutional Resources

		IND/IDE—Suzan Moser, MBA, Clinical Research Specialist, School of Medicine, Washington University, St. Louis
		What to do when YOU are the Sponsor—Laura Herbelin, Clinical Trial Research Consultant
		HOPE—Kathleen Quinn, PhD, Associate Dean for Rural Health and Director of the Rural Scholars Program, MU School of Medicine
		IRB—Lori Wilcox, PhD, Director, Compliance, MU
		RII—Christine Terry, PhD, Director of Professional Development, MU
		OSPA—Brenda Leuenberger, Associate Director, Pre-Award, Office of Sponsored Programs Administration, MU
		Grant Writing—Charlene Emerson, PhD, Lead Grant Writer, NextGen Precision Health, MU
		Library Resources—Rachel Alexander, MLIS, Health Sciences Library Research Support Librarian, MU