A full day training designed to provide basic knowledge that is beneficial for research coordinators and staff. The program includes lectures, interactive activities, and breakout group exercises.
The Clinical Research Study Coordinator Bootcamp will include one full day of in-person, highly interactive programming, complemented by approximately eight hours of didactic content delivered online through a Canvas course.
The program is designed to provide basic knowledge that is beneficial for research coordinators and staff. The program includes lectures, interactive activities, and breakout group exercises.
By the end of this course, learners should be able to:
- Define the responsibilities of a clinical research coordinator.
- Understand the principles of good clinical practice.
- Understand best practices for study start up, conduct and closeout.
- Understand the resources available to assist with clinical trials at the institutional level.
A Clinical Research Study Coordinator Bootcamp certificate will be provided to those who complete all course modules.
For additional information, please reach out to Veronica Lemme at lemmev@health.missouri.edu.
Details:
- March 6, 2026, 8 a.m- 4 p.m.
- Location: Tom and Linda Atkins Family Seminar Room, Roy Blunt NextGen Precision Health building, Columbia, Mo.
- In-person only
Register Here
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Canvas Course Modules
- Scope & Importance of Clinical Trials
- Documenation
- Recruitment & Retention
- Informed Consent
- Study Start-up (Budgets & Contracts)
- Research Integrity & Compliance (COI)
- Study Conduct & Close Out
- IDS Pharmacy
- IRB
- PI & CRC Responsbilities
- Working with Study Monitors
- FDA, IDE & IND Studies
- Coverage Analysis
- OnCore
In-Person Agenda (Friday, March 6)
- Overview of Canvas Content
- Protocol Breakdown
- Time Management
- Safety & Adverse Event Reporting
- Between Compassion & Compliance: Ethics in Research panel discussion
- Consenting & Non-Compliance Scenarios
- Good Clinical Practice
- Lab Management
- ClinicalTrials.gov
- Break Outs (Filling out the IRB Application, Budgeting for your Trial)
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Reviewed 2026-01-13