Therapeutic Areas

Cardiology/Vascular Diseases
Dental and Oral Health
Dermatology
Endocrinology
Family Medicine
Gastroenterology
Hematology
Immunology
Internal Medicine
Musculoskeletal
Nephrology
Neurology
Obstetrics/Gynecology (Women’s Health)
Ophthalmology
Orthopedics/Orthopedic Surgery
Pediatrics/Neonatology
Pulmonary/Respiratory Diseases
Rheumatology
Vaccines

Center Overview

Pharmaceutical Research Organization, a Trial Management Organization, offers a diverse arena of clinical trial capabilities including pediatric and adult outpatient, as well as inpatient, studies. We pride ourselves in delivering timely, accurate and reproducible results to sponsor companies and Clinical Research Organizations. We insist on producing work of only the highest caliber. Sponsors and CROs have the ability to reach our administrative officers, or any of our trained study coordinators, 24 hours a day, 7 days a week. Our goal is to make the entire clinical trial process smooth from beginning to end by placement, Principal Investigator recruitment and training, contract and budget negotiation, regulatory affairs, coordinator assignments, patient recruitment, data collection, quality assurance and compliance.

Pharmaceutical Research Organization's Mission Statement:

Pharmaceutical Research Organization’s mission is to improve health care locally and globally by managing clinical trials in a prompt, efficient manner and to the highest quality standards.

We treat our customers – pharmaceutical companies, CROs, investigators and their clinic staff and patients, as well as our employees with the utmost respect and professionalism.

We provide the best possible experience for our customers during the clinical trial process and accept no excuses for less than outstanding service and resolution to all issues – predicted or unforeseen.

Clinical Research Experience

Pharmaceutical Research Organization has established relationships with a wide range of specialty practices. We will also recruit additional Principal Investigators and sites, as well as place trained and research-dedicated study coordinators at those sites, for almost any other specialty or practice to meet sponsor requirements or protocol-specific needs. For a more detailed listing of Pharmaceutical Research Organization’s Clinical Research Experience, please visit our web page www.pharmaceuticalresearchorganization.com.

Sponsors and CROs Pharmaceutical Research Organization has contracted with include:

Sponsors:

CROs:

Clinical Trial Research Experience Drug Category:

Facility Description

To date, Pharmaceutical Research Organization has contracted with 81 pharmaceutical companies, 48 Contract Research Organizations, over 47 independent and private-practice Principal Investigators, and 31 investigative sites to conduct 442 research studies and enroll over 13,000 patients throughout the state of Utah.

Investigator Experience

Investigative sites include, but are not limited to the following areas of specialty:

Staff Expertise

Pharmaceutical Research Organization is comprised of trained coordinators with over 37 years combined coordinator research experience.

A special note about our Clinical Research Coordinators:
Our coordinators are research-dedicated. They consist of mostly full-time and a few part-time employees. Their backgrounds include RN, LPN or CMA degrees as well as ACRP and SOCRA certifications. These research-trained and dedicated coordinators are placed at our investigational sites to assist the investigators in recruiting, screening, enrolling and gathering data on each of our contracted protocols to help ensure GCP/ICH compliance and high, quality enrollment.

Patient Demographics

Composition by race (site dependent):

Caucasian 80%
African-American 5%
Asian 5%
Hispanic 5%
Other 5%

Composition by gender:

Male 50%
Female 50%

Other Information

Pharmaceutical Research Organization uses a Central IRB.

Pharmaceutical Research Organization Conducts Mainly Phase II-IV Clinical Research Protocols.

Pharmaceutical Research Organization has established relationships with a wide range of specialty practices. We will also recruit additional Principal Investigators and sites, as well as place trained and research-dedicated study coordinators at those sites, for almost any other specialty or practice to meet sponsor requirements or protocol-specific needs.

Contact Center

If you are interested in contacting this center to discuss placing a clinical trial there, please complete and send the email form below. A representative from the research center will then follow up with you.