Summary
Overview
Work History
Education
Skills
Timeline
Generic

Glinda Thomas

Flora,MS

Summary

Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning. Equipped with strong problem-solving abilities, willingness to learn, and excellent communication skills. Poised to contribute to team success and achieve positive results. Ready to tackle new challenges and advance organizational objectives with dedication and enthusiasm.

Overview

17
17
years of professional experience

Work History

Clinical Research Coordinator

Olive Branch Family Medical Center
07.2023 - Current
  • Managed patient recruitment, informed consent process and data entry to support trial objectives.
  • Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
  • Gathered, processed, and shipped lab specimens.
  • Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
  • Collected, evaluated, and modeled collected data.
  • Complied with research protocols by providing ongoing quality control audits.

Clinical Research Coordinator

Precise Clinical Neuroscience Specialist
11.2022 - 07.2023
  • Followed informed consent processes and maintained records.
  • Maintained accurate and up-to-date case report forms and source documents for traceability.
  • Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
  • Monitored unit budget to meet financial objectives for spend rate and funding.
  • Prepared and maintained regulatory documents for clinical trial submissions.
  • Monitored patient safety throughout clinical trials and reported any adverse events.

Clinical Research Coordinator

Jackson Arthritis Clinic
06.2008 - 11.2022
  • Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
  • Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
  • Monitored patient safety throughout clinical trials and reported any adverse events.
  • Facilitated focus group sessions with project patients.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Collected data and followed research protocols, operations manuals, and case report form requirements.

Education

Bachelor of Science - Health Sciences

Grand Canyon University
Phoenix, AZ

Associate of Science - Medical Office Management

Virginia College
Jackson, MS

High School Diploma -

Madison Central High School
Madison, MS

Skills

  • Quality Assurance
  • Problem-solving skills
  • Microsoft Word
  • MS office
  • Analytical thinking
  • Conflict resolution
  • Medical Billing
  • ICD-10
  • Adaptability and flexibility
  • Insurance Verification
  • High-energy attitude
  • CRM software
  • Member account management
  • Relationship building
  • Microsoft Excel
  • Problem-solving
  • Call escalation
  • Compliance management
  • Documentation review
  • Policy interpretation

Timeline

Clinical Research Coordinator

Olive Branch Family Medical Center
07.2023 - Current

Clinical Research Coordinator

Precise Clinical Neuroscience Specialist
11.2022 - 07.2023

Clinical Research Coordinator

Jackson Arthritis Clinic
06.2008 - 11.2022

Bachelor of Science - Health Sciences

Grand Canyon University

Associate of Science - Medical Office Management

Virginia College

High School Diploma -

Madison Central High School

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