1816 W. Mount Vernon St. Springfield, MO 65802, USA

Careers

Click here for a comprehensive look at the QPS Missouri site located in Springfield, Missouri

Years Serving Clients

240

Clinical Trials Beds

Successful FDA Inspections

1,500

Clinical Studies Completed

QPS Missouri: You Can Make A Difference

QPS Missouri: How Should I Prepare for my Screening?

QPS: Missouri Virtual Campus Tour

Why Choose QPS Missouri

Participating In A QPS Missouri Clinical Study – 1

Participating In A QPS Missouri Clinical Study – 2

QPS Missouri

QPS Missouri offers a broad range of services to support drug development research, and to design and conduct Phase I clinical studies.
Established in 1994, QPS Missouri is located on a 5-acre, independently-owned campus, with 80+ employees.

QPS Missouri Clinical Site Overview

The QPS Clinical Research site in Springfield, MO, USA is an impressive facility in a great location. If you are a sponsor looking for a site, or a potential study subject looking to participate in a clinical trial, this interactive resource provides a closer look at the facility and surrounding area.

2020 Sponsor Booklet

Core Competencies

Phases I and II Clinical Studies.
- Smoking Cessation.
- Vaccines.
- Women’s Health.
- Bioavailability.
- Bioequivalence.
- Nutrition.
Data management.

Facility

240 beds across 5 updated clinical units designed for open-concept layout.
24-hour security systems and automatic natural gas-powered generators for power backup.
Secure on-site archive/document storage with FM-200 gas fire suppression.
Laminar flow hoods; -70˚C and -20˚C freezers.
14 micro-, table-top, and floor centrifuges, and high-speed micro-centrifuges.
National Institute of Standards and Technology (NIST) calibrated temperature recording devices in refrigerators and freezers.
Secure pharmacy and retention with DEA-approved safe for Schedule I-IV drugs.
Local clinical lab provides most results within 24 hours, 7 days a week.

People

Highly experienced principal investigators (PIs) with as much as 20+ years’ experience in clinical research.
Leadership team includes technology and CRO services experts with 20+ years of experience.
Average management team experience includes 10+ years in CRO.
Dedicated Institutional Review Board (IRB) conducts reviews in accordance with pertinent authorities, including ICH E6: Good Clinical Practice Consolidated Guidance; US FDA (21 CFR Parts 50 and 56); and the US Department of Health.