Overview

AMR LRC, a trial management organization, offers a diverse arena of clinical trial capabilities including pediatric and adult outpatient and 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 can reach our administrative officers or any of our trained study coordinators 24 hours a day, seven 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.

Our Mission

To conduct high quality, ethical clinical research with patient welfare at the forefront of all we do. Our efforts drive development of medical cures and treatments of tomorrow, while fostering person growth for team members and positively impacting our communities.

Our Vision

To become the largest, most respected, innovative and highest quality clinical research company dedicated to improving health-worldwide.

Our Values

EXCELLENCE

- Strive for excellence and consistency in every type of research we do.

INNOVATION

- Find innovative and ground-breaking solutions through collaboration.

RESPECT

- Treat everyone - subjects, sponsors and associates - with respect.

COMMUNITY

- Base decisions and growth on striving to build a better community.

ETHICS

- Make the right and honorable decision even if it is the hard or costly one.

Research Experience

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

AMR Utah conducts mainly phase 2 to 4 clinical research protocols. For a more detailed listing of our clinical research experience, please visit our web page, www.amrlayton.com.

Sponsors and CROs AMR Utah has contracted with include:

Sponsors

CROs

Clinical trial research experience by drug category

To date, AMR Utah has contracted with 90 pharmaceutical companies, 50 contract research organizations, more than 47 independent and private-practice principal investigators, and 30-plus investigative sites to conduct 450 research studies and enroll more than 16,000 patients throughout the states of Utah and Idaho.

Facility Description

AMR LRC is located in the heart of Holy Cross Hospital medical campus in Layton Utah.

Our Facility Includes;

• DEDICATED RESEARCH EXAM ROOMS
• ON-SITE LAB AND PROCESSING
• INPATIENT AND OUTPATIENT
• ECG MACHINES, X-RAY, AND DEXA SCANNING
• DOUBLE-LOCKED DRUG STORAGE
• CLIMATE-CONTROLLED ARCHIVAL
• -20° AND -70° REFRIGERATION AND DRY ICE
• 24HR ABPM EQUIPMENT
• EMERGENCY EQUIPPED WITH BACK-UP POWER
• PRIVATE AREAS FOR MONITORS
• SPIROMETRY AND INFUSION PUMPS
• AMBIENT AND REFRIGERATED CENTRIFUGES

Investigator Experience

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

Staff Expertise

AMR Utah is comprised of trained coordinators with more than 40 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