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