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About Pantheon Clinical Research

At Pantheon Clinical Research, our mission is to advance medical knowledge through dedication, experience, and unwavering commitment to ethical standards.

About Pantheon Clinical Research

At Pantheon Clinical Research, our mission is to advance medical knowledge through dedication, experience, and unwavering commitment to ethical standards.

Who we are

About Our Facility

The team at Pantheon Clinical Research boasts more than three decades of extensive experience in the clinical trial industry. Our strategically situated facility in Bountiful, Utah, a mere 10-minute drive north of Salt Lake City, spans approximately 2,000 square feet. It features fully equipped examination rooms, spacious areas designated for meticulous rating scale assessments, and dedicated monitor workspaces.

We provide a state-of-the-art double-locked investigation product storage room equipped with high and low-temperature monitoring systems, ensuring the utmost security and compliance.
our mission
PANTHEON CLINICAL RESEARCH is dedicated to conducting clinical research with unwavering commitment to ethical standards, advancing medical knowledge and improving healthcare outcomes.

About our team

OUR TEAM AT
PANTHEON CLINICAL RESEARCH

Our Team at Pantheon Clinical Research comprises dedicated professionals who bring a wealth of experience and expertise to the forefront of our mission. Committed to advancing medical knowledge and ensuring the highest standards of research ethics, our diverse team collaborates seamlessly to drive innovation in clinical trials. Get to know the individuals who make up our dynamic and passionate team, each contributing their unique skills and insights to our collective pursuit of excellence in healthcare research.

Dr. Jackson Rhudy

Principal Investigator

Dr. Jackson Rhudy

Principal Investigator

Dr. Jackson Rhudy, our highly regarded Principal Investigator has an impressive three-decade career in clinical trials. His unwavering commitment to research ethics is evident in his flawless regulatory compliance record. Dr. Rhudy’s unblemished reputation and dedication to scientific excellence are further reflected in his never having faced debarment. As a stalwart figure in the industry, his leadership drives our commitment to excellence and innovation in clinical trials.

Our Pl, Dr. Rhudy, has been conducting clinical trials for the last 30 years, and he is well-known in the industry. He has never received a 483 and has never been debarred.

Mari Livermore

Site Director/CEO

Mari Livermore

Site Director/CEO

Mari Livermore, our esteemed Site Director and CEO, stands as a pillar of experience and leadership in the clinical research industry. With an impressive career spanning over three decades, Mari has traversed the realm of clinical trials both as a meticulous monitor and as a discerning auditor.

Her journey through diverse roles has equipped her with a profound understanding of the industry’s intricacies, enabling Pantheon Clinical Research to flourish under her guidance. Mari’s unwavering commitment to Good Clinical Practice (GCP) compliance, timely query resolution, precise data entry, and comprehensive source documentation reflects her dedication to research integrity.

Mari’s visionary leadership drives our mission of excellence and innovation in clinical research, fostering an environment where every study thrives.

Jon Purcell

Director of Operations

Jon Purcell

Director of Operations

Jon Purcell is a dynamic and results-driven professional, infusing Pantheon Clinical Research with his passion for orchestrating successful clinical research operations. Armed with a background in software systems and financial management, Jon brings a unique and valuable perspective to our team. His strategic insights and keen organizational skills are instrumental in advancing the growth and success of our clinical research endeavors. Jon’s innovative thinking and commitment to efficiency enable us to navigate the complex landscape of research with precision and effectiveness, ultimately contributing to our mission of expanding medical knowledge and improving healthcare outcomes.

 

How we work

Comprehensive Pre-Screening and GCP Compliance

Our meticulous subject pre-screening process commences promptly, well in advance of the actual screening date, typically 1 to 2 weeks ahead. At this initial visit, subjects receive the study consent form for review at home, contributing to our remarkably low screen-failure and early-termination rates, setting us apart from other sites.

Recognizing the significance of adhering to timelines, especially when onboarding new sites, we are committed to efficient operations.

Furthermore, our Site Director's extensive background as an FDA auditor and monitor underscores Pantheon Clinical Research's profound commitment to GCP compliance, timely query resolution, database integrity, accurate data entry, and rigorous source documentation. With vigilant PI oversight and an unwavering focus on maintaining a low screen-failure rate, compliance remains at the forefront of our priorities.

Get in touch with us today.

Ready to take the next step or have questions? Contact us today to connect with our experienced team and explore how Pantheon Clinical Research can be your partner in groundbreaking medical research.
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