Sponsors/CROs
Rapid Study Start-Up
Quality Clinical Research, Inc has processes in place to efficiently turn around initial documents in less than one week. Site staff prepares the regulatory packet for time-sensitive start-up activities. Contracts and budgets are negotiated in-house which allows for faster turnaround.
Speedy Recruitment and Retention
Our full-time Recruiting Specialist develops recruiting and screening strategies while waiting for IRB approval. That way we can kick-off recruitment efforts and start scheduling screenings as soon as IRB and Sponsor approval is granted. We have thousands of volunteers in our patient database. Our full-time Recruiting Specialist carefully reviews selection criteria to ensure a higher probability of study completion. We regularly follow up with patients to ensure compliance with study requirements and appointments. We pride ourselves on our history of exceeding enrollment goals. Our retention rate is 90%.
Clean Data
We are able to deliver clean data to clients because of GCP, ICH and FDA 21CFR compliance. Our well established standard operating procedures ensure study success, low query rates and favorable audits. We frequently have the lowest number of queries per study among multiple sites.
Source Preparation
FDA-auditable source documents are prepared on site. QCR creates separate source documents for each visit that are user-friendly. All procedures and information are organized by collection date per protocol requirements. Our Data Entry Specialist is trained on most EDC system and enters source documents within 48 hours of the subject’s visit. QCR can create source for your next clinical trial. Please contact Tricia Harrison at tricia@qcromaha.com.
Our facility is conveniently located in Omaha, Nebraska—just off interstate 680.
• Less than 15 minutes from the heart of downtown Omaha
•About 20 minutes from the airport
1.2 million residents within a 50 mile (80 km) radius of the city’s center, forming the Greater Omaha area.
Racial Composition
Caucasian 60%
African-American 25%
Asian 1%
Hispanic 12%
Other 2%
All members of our coordinating staff are certified in the following:
We currently employ 5 full-time research coordinators, 1 full-time regulatory assistant, 2 full-time assistant research coordinators, and 1 full-time patient recruiter.
Taken together, our staff has contributed to the operation of over 300 clinical trials and has research coordinating experience in the following indications:
