FOR SPONSORS/CROS
BECOME PART OF THE CRS TEAM
FOR SPONSORS/CROS
BECOME PART OF THE CRS TEAM
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.

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Physician Investigators from all Therapeutic Backgrounds
Allergy / Immunology
Dermatology
Family Medicine
Gastroenterology
Internal Medicine
Orthopedics
Rheumatology
Urology Vaccines
BPH
Experience in Therapeutic areas
Acne
Allergies
Arthritis (OA, RA)
Asthma
Athlete’s Foot
BPH
Bronchitis
Cholesterol
COPD
Dermatitis
Diabetes I & II
ED
Generally Healthy
Gout
Headache
Heartburn
Hypertension
IBD (Crohn’s)
Influenza
Obesity
Osteoporosis
Overactive Bladder
Prostate Cancer
Psoriasis
Ulcerative Colitis
Urinary Tract Infection
Vaccines
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.
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.
