Expert Research Management

At TMA, we partner with private physician practices to successfully manage and execute Phase II-IV industry sponsored clinical research studies.

Our vast, experienced network of seasoned Principal Investigators allows Sponsors and/or Clinical Research Organizations (CROs) to reduce the time and resources required to identify, screen and qualify Investigators. In addition, our coverage allows Sponsors access to a large and diverse patient population. TMA manages and coordinates all aspects of the clinical trials to ensure accurate and timely results.

Proper Site Management is a critical component of the trial. We are meticulous in ensuring that each site follows the proper site protocol. Each site is assigned a Project Manager and Clinical Research Coordinators to work with the Investigators to provide our Sponsors efficient, high quality research results.

Trial Management Associates

Working with us has its advantages.

TMA offers:

  • Dedicated, experienced, full-time Clinical Research Coordinator/s at each site
  • Experienced employees in regulatory documentation preparation and maintenance
  • Excellent track record of meeting and exceeding patient recruitment goals
  • Strong working relationships with our sponsors and IRBs
  • Clinical Research supporting the ICH-GCP and HIPPA guidelines
  • Good Clinical Practice (GCP) training for Investigators and staff
  • Quality data management for clinical research sites

Therapeutic Areas
We focus our research on several key therapeutic areas, including:

  • Vaccines
  • Family Medicine/Internal Medicine
  • Nephrology
  • Gastroenterology
  • Infectious Disease
  • Endocrinology
  • Dermatology
  • Pulmonolgy
  • Cardiology
Trial Management Associates Wilmington NC

Advancing Medicine. Improving Lives.

Have a question? We’d like to hear from you.

(910) 833-1954

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