Summary
Overview
Work History
Education
Skills
Leadership & Honors
Timeline
Generic

CARLTON THOMAS

Memphis,TN

Summary

Healthcare and research professional with hands-on involvement in clinical trial workflows, study visit support, specimen collection, IATA-compliant specimen shipping, EDC data review, query resolution, protocol compliance, participant recruitment, informed consent, and regulatory documentation. Currently completing an MPH while supporting clinical research activities in a urology research department and performing delegated responsibilities on an industry-sponsored Phase III clinical trial. Brings a strong blend of clinical experience, research methodology, and public health training to clinical research coordination roles.

Overview

4
4
years of professional experience

Work History

Medical Assistant

Conrad Pearson / Austin Urology
Memphis, TN
06.2026 - Current
  • Prepare 4 procedure rooms per shift to support examinations and maintain smooth patient flow.
  • Track 25-30 patient intake records daily while keeping visits organized and documentation complete.
  • Maintain accurate EMR documentation and communicate relevant patient updates to providers.
  • Coordinate patient care activities and follow-up while supporting organized clinic operations.
  • Support confidentiality and protocol adherence throughout patient interactions and daily workflow.

Clinical Research Practicum

Austin Urology / Conrad Pearson
Memphis, TN
08.2026 - 10.2026
  • Supported 3-5 study visits per week while completing protocol-specific procedures under CRC supervision.
  • Reviewed and resolved EDC queries, then joined monitor discussions to support data accuracy and protocol compliance.
  • Performed sponsor-specific clinical trial procedures under CRC supervision while following study workflows and regulatory requirements.
  • Documented delegation status for the Phase III Telix BIPASS Trial and followed the Flow Stent trial to learn visit structure and operations.
  • Developed a Clinical Research Operations Assessment and a toolkit with workflow checklists, recruitment resources, and informed consent materials.
  • Created regulatory binder templates and quick-reference guides to strengthen source documentation and study-ready organization.

Research Intern

Mississippi INBRE Program
Ridgeland, MS
05.2024 - 07.2024
  • Coordinated research initiatives and community health engagement activities to keep study work moving on schedule.
  • Collected clinical and behavioral data for ongoing research activities, supporting clean and consistent dataset development.
  • Facilitated communication between research teams and community partners while preparing reports and project materials.

Undergraduate Researcher / Study Lead

Ronald E. McNair Scholars Program / University of Southern Mississippi
Hattiesburg, MS
12.2022 - 12.2023
  • Supported study participants through consent, intake, and data collection for the maternal mortality project.
  • Developed study protocols and prepared IRB submissions for an IRB-approved human-subjects study on maternal mortality disparities.
  • Recruited participants, obtained informed consent, and collected demographic, clinical, and behavioral data using validated instruments.
  • Maintained source documentation and followed approved study procedures to support compliance and data integrity throughout the project.
  • Conducted literature reviews and contributed to abstracts, presentations, and conference dissemination of study findings.
  • Tracked study activities and resolved queries across records to keep research operations organized and audit-ready.

Education

Master of Public Health - Urban Health

University of Memphis
Memphis, TN
12-2026

Bachelor of Science - Health Sciences, Chemistry, Public Health, Psychology

University of Southern Mississippi
Hattiesburg, MS
12-2024

Skills

  • Clinical trial workflows
  • Study coordination
  • Informed consent
  • Participant recruitment
  • Source documentation
  • IATA-compliant specimen shipping
  • EDC data management
  • Query resolution
  • Protocol compliance
  • Regulatory documentation
  • IRB submissions
  • Good clinical practice
  • Human subjects research
  • Adverse event reporting
  • Serious adverse event reporting
  • Protocol deviation tracking

Leadership & Honors

Ronald E. McNair Scholar, Mississippi INBRE Health Scholar, President, Minority Association of Pre-Medical Students (MAPS)

Timeline

Clinical Research Practicum

Austin Urology / Conrad Pearson
08.2026 - 10.2026

Medical Assistant

Conrad Pearson / Austin Urology
06.2026 - Current

Research Intern

Mississippi INBRE Program
05.2024 - 07.2024

Undergraduate Researcher / Study Lead

Ronald E. McNair Scholars Program / University of Southern Mississippi
12.2022 - 12.2023

Bachelor of Science - Health Sciences, Chemistry, Public Health, Psychology

University of Southern Mississippi

Master of Public Health - Urban Health

University of Memphis