Courtney Pinto
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Courtney Pinto

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Credential Verification

Issue date: July 30, 2026

ID: 28e534cc-20cb-4c14-8fb3-5531331934ef

Issued by

UT San Antonio Research & Innovation

UT San Antonio Research & Innovation provides resources and infrastructure for research conducted across UT San Antonio, UT System, and other research partners.

Type

Training

Level

Introductory

Format

Offline

Duration

15 hours

Price

Free

Description

The Clinical Research Development Workshop is an educational workshop for research coordinators and study staff, developed by the Research Administration and Quality Office, a division of Research & Innovation at UT San Antonio Health Science Center. The Workshop is a hands-on, two-day program designed to give early-career research staff the foundation they need to successfully manage clinical research studies at UT San Antonio Health Science Center. Topics covered in the Workshop include evaluating a research proposal for feasibility, applying for IRB and institutional approval to conduct human research, working with the Clinical Trials Office to develop a coverage analysis and budgets, creating and maintaining study regulatory binders and essential documents, recruiting and retaining research participants, obtaining informed consent from research participants, determining whether a participant qualifies for study enrollment, managing research participant payments, tracking research visits in the Velos eResearch clinical trial management system, evaluating and reporting unexpected problems and noncompliance, working with monitors, auditors, and inspectors, and closing out research studies and archiving study records.

Skills

Evaluating a research proposal for feasibility

Applying for IRB and institutional approval to conduct human research

Working with the Clinical Trials Office to develop a coverage analysis and budgets

Creating and maintaining study regulatory binders and essential documents

Recruiting and retaining research participants

Obtaining informed consent from research participants

Determining whether a participant qualifies for study enrollment

Managing research participant payments

Tracking research visits in the Velos eResearch clinical trial management system

Evaluating and reporting unexpected problems and noncompliance

Working with monitors, auditors, and inspectors

Closing out research studies and archiving study records

Earning Criteria

Participation

Individuals who earn this certificate have satisfied the expectations of the Clinical Research Professional Development Workshop by attending and participating in a two-day, in-person workshop. Certificate holders have invested approximately 14.5 hours to meet course requirements.