Why Choose CRS?

FOR SPONSORS/CROS

– PHASE II-IV CAPABILITIES

We pride ourselves on having a combined total of over 150 years of phase IV clinical research experience. We have conducted multiple Phase II “first in human” trials and have the ability to run inpatients visits for 2 weeks or more at a time.

– FASTER START-UP TIMES

Our unique business model allows us to negotiate a single contract and budget for multiple sites selected on a single protocol. This drastically cuts down the negotiation and start-up time for the sponsor, and gives our sites more time than competitors to enroll patients. Additionally, we cooperate as a group to share resources like source documentation which further cuts down on our individual site start-up timelines.

– BETTER PATIENT RECRUITMENT

We play by the numbers: more sites equates to more patients, particularly when sites are working together towards the same goal.

FOR PHYSICIANS

Give your current patients access to novel treatment options and expand your practice and reputation by taking part in ongoing cutting-edge research. Chase your scientific interests and potentially be part of the next breakthrough, all while earning additional compensation for seeing patients you already regularly treat in your practice.

Clinical Trial Experience

CRS conducts Phase II-IV clinical trials for both pharmaceutical companies and contract research organizations. Our research sites have earned a reputation for excellence, as they consistently reach and exceed the expected recruitment and randomization goals with qualified compliant study patients.

We have been recognized on numerous occasions for having the highest enrollment.

Due to rigorous and careful screening, our sites have enjoyed high completion rates with minimal numbers of screen failures. We accurately document all study procedures, tests, and events all while maintaining complete source documents and timely completion of protocol required documentation.

CRS has three locations conveniently located throughout Florida, Ohio, and Tennessee. This allows us to be strategically positioned to offer services to the immediate medical community as well as outlying rural communities.
We are closely aligned with physician practices throughout the region and the number of patients referred by our physicians nearly unheard of in the industry.

Our experienced clinical operations team will expertly manage all of the aspects of your trial. With a serious commitment to timelines, the critical importance of accuracy and adherence to protocols.

CRS has dedicated QA, Training, Regulatory and Contracts & Budget staff.

Clinical Trial Experience

Clinical Research Solutions maintains a unique collaboration with physician’s practices and urgent care centers conducting thousands of patient visits a year. These centers are an excellent recruitment source for filling your trials recruitment needs.

Database

Clinical Research Solutions began using Clinical Conductor™, a clinical trial management system (CTMS), allowing us to track virtually every aspect of the trial from the time our site was selected through close-out of the trial. This can include, but is not limited to, the effectiveness of advertisements; demographics of the study population; numbers of potential participants with a specific diagnosis; taking specific medications and/or lab criteria; screen failure rates; time studies and much more.

Investigators

Clinical Research Solutions has an ongoing relationship with a number of family practitioners, urologists, internists, pulmonologists and other specialists who participate as principal investigators or sub-investigators.

Full-time Patient Recruitment Department

A major component of our enrollment success is our utilization of full-time dedicated recruitment department. Recognizing the critical importance of study timelines, our recruitment team is well versed and can help you every step of the way in order to ensure a timely enrollment.

Commitment & Quality

At Clinical Research Solutions, we are committed to providing you with quality research. We understand the importance of timelines; the critical need for accuracy and adherence to protocol. Our proven track record to demonstrates our ability to meet all of your needs.

Prompt turnaround on budget and contract negotiations

Regulatory submissions quickly and accurately

Ability to use Central IRB

Quick and efficient start-up

Meet or exceed contractual enrollment numbers

AFFILIATES MEMBERS OF: