Coordinator Training

Research Coordinator Training Resources

• Minimum Training Requirements for Clinical Research Staff  (updated 08/18/2017)
• Nurse Researcher/Clinical Research Coordinator Orientation Checklist (updated 08/18/2017)

Research Coordinator Meetings

Upcoming Meetings

Date	Time	Location	Topic	Speaker
6/21/2018	12:00 - 1:00	STC 5051 A, B, & C	Electronic Regulatory Binders	QA/QI Program
7/18/2018	12:00 - 1:00	Morsani 1013 A & B	Conflicts of Interest in Research	COI Program
7/19/2018	12:00 - 1:00	STC 5051 A, B, & C	Conflicts of Interest in Research	COI Program
8/15/2018	12:00 - 1:00	Morsani 1013 A & B	Ceding Review to External IRBs	Research Integrity & Compliance
8/16/2018	12:00 - 1:00	STC 5051 A, B, & C	Ceding Review to External IRBs	Research Integrity & Compliance

Past Meetings

• May 2018 - CTMS as a Research Participant Recruitment Database
• April 2018 - ClinicalTrials.gov
• March 2018 - Infection Control, Biomedical Waste, PPE, & Reporting Exposures
• February 2018 - Compliant ClinCard Processes
• January 2018 - Revised ICH-GCP E6 Guidelines
• November 2017
  • How to Schedule Research Study Visits in the USF Instance of Epic and Avoid Billing Noncompliance
  • Common Rule Revisions
• October 2017 - Common Rule Revisions
• August 2017 - USF Investigational Pharmacy P&Ps
• July 2017 - USF IRB Submissions
• November 2016 - Study Closure
• July 2016 - Working with Schulman IRB & Updates on HSP Regulations
• August 2015 - Preparing for an IRB Audit
• July 2015 - ACRP
• March 2015 - Quality Assurance
• February 2015 - Overview of Shulman IRB
• January 2015
  • Study Coordinator - COI
  • ROAD OFA
• November 2014 - Strategies to Prevent FDA Inspection Findings
• October 2014 - OCR Processes and Procedures
• August 2014 - Investigator Initiated Research
• June 2014 - Quintiles Partnership
• May 2014 - Capturing and Reporting Adverse Events
• April 2014 - After IRB Approval
• March 2014 - Risk Management
• January 2014 - Documentation of Research Records and HIPAA
• December 2013 CRC Meeting Material - Highlights From the SoCRA FDA Clinical Trial Requirements, Regulations, Compliance and GCP
• November 2013 CRC Meeting Material - Intricacies of the IRB Application
• October 2013 CRC Meeting Material - Obstacles to Enrollment
• September 2013 CRC Meeting Material - R.O.A.D. Training
• August 2013 CRC Meeting Material - Minimum Training Requirements for Clinical Research Staff
• June 2013 CRC Meeting Material - Commercial IRB Submission Process: Lessons Learned
• May 2013 CRC Meeting Material - Good Clinical Practices (GCPs)
• February 2013 CRC Meeting Material - ClinicalTrials.gov
• December 2012 CRC Meeting Material - Brief OCR Updates
• June 2012 CRC Meeting Material - Hot Topics
• May 2012 CRC Meeting Material - Accessing the OCR SharePoint PI Protocol eLibrary
• April 2012 CRC Meeting Material – ClinCard: Instant Automated Patient Payments and Messaging
• February 2012 CRC Meeting Material - SOP: Recruitment & Advertising in USF Health Clinic Waiting Areas
  • February 2012 CRC Meeting Supplemental Material - Florida Clinical Trials, a New Approach
• December 2011 CRC Meeting Material - OCR "State of the Office"
  • December 2011 CRC Meeting Supplemental Material - Florida Clinical Trials Update
• November 2011 CRC Meeting Material - Study Participant Registration & Billing
• October 2011 CRC Meeting Slides - Update to the Study Status Log Submission Process
• September 2011 CRC Meeting Slides - OCR Website Navigation: A Virtual Tour
• August 2011 CRC Meeting Slides - Updates to the WIRB Submission Process
• July 2011 CRC Meeting Slides - Internal Form and Clinical Trial Contracts Training