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Office of Clinical Research

Coordinator Training

Upcoming Meetings

Office of Clinical Research Overhead - What is it used for?

Speaker: Dawn Carnegie

Date: January 17, 2020
Time: 11am - 12pm
Location: Morsani 1013B

Research Coordinator Training Resources

    • November 2019 - USF IRB External Application - Changes with the Process
    • September 2019 - ACRP & SOCRA: Membership and Certification Opportunities
    • August 2019 - Social Media & Other Recruitment Methods
    • May 2019 - Research Billing Compliance for UMSA Services
    • March 2019 - Back to Basics: Scheduling/Prepping Visits
    • February 2019 - Back to Basics: Scheduling/Prepping Visits
    • January 2019 - Back to Basics: Lab Processing
    • December 2018 - Back to Basics: Regulatory
    • November 2018 - Back to Basics: Source Documentation
    • October 2018 - Back to Basics: The ICF Process
    • August 2018 - Ceding Review to External IRBs
    • July 2018 - Conflicts of Interest in Research
    • June 2018 - Electronic Regulatory Binders
    • 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