Our Clinical Study Services

AMR Clinical performs all phases of clinical research trials to support biopharmaceutical and medical device companies in the development of new drugs, devices, and diagnostics. Our flexible clinical study services propel clinical trials from ideas to reality through relationships with industry leading companies.

RESEARCH DONE RIGHT

The AMR Clinical Difference

Clinical Research Experts

  • Thought leaders in clinical research 
  • Teams of specialist investigators, licensed pharmacists
    and pharmacy technicians, and credentialed laboratory staff 
  • Clinical research support teams experienced in
    supporting specialized care and procedures 
  • Dedicated Patient Experience team 
  • Dedicated centralized contracting, project management,
    regulatory, start-up teams, and data management teams
  • Committed to delivering quality and excellence
Two lab professionals—one younger Asian woman and one older Caucasian woman—both in white coats and blue gloves, seated at a desk, leaning in and pointing at a large desktop monitor as they discuss their data.

Industry Leading Capabilities

  • Controlled substance licenses 
  • Advanced imaging and diagnostic capabilities 
  • Local PBMC processing capabilities 
  • Local Institutional Biosafety Committees 
  • Live-attenuated vaccine handling 
  • Biosafety Level II cabinets 
  • Biosafety Level I & II certifications 
  • Sterile drug preparation environments 
  • Federal Wide Assurance (FWA) numbers 
A close-up of a young woman scientist in a white lab coat and blue gloves, wearing clear safety goggles, using a pipette to transfer liquid into a petri dish at a microscope station, with another researcher blurred in the background.

Clinical Research Enrollment and Retention

  • Both rapid enrollment and superior participant retention 
  • Industry leading clinical trial enrollment and retention statistics
  • Actively engage communities, providing access to diverse participant populations
A middle-aged man with salt-and-pepper hair, beard, and black-frame glasses sits at a wooden kitchen table, holding a smartphone in one hand and a white coffee mug in the other, smiling as he reads from his phone.

Focused Recruitment

  • Private practice access for participant-flow and database mining 
  • Innovative recruitment with customized recruitment plans per study leveraging real world data and insights
  • Adjacency and partnerships with leading medical facilities in each market 
  • Regularly scheduled community outreach and education programs
  • Customized local media campaigns 
  • Dedicated participant recruiters 
  • Media, PR, and marketing specialists 
A friendly interaction at a clinic reception desk: a female medical receptionist or nurse (in light blue scrubs) gestures with her hands while speaking to a smiling male patient standing on the other side, with a computer monitor and appointment calendar visible in the foreground.

Equipped to Exceed Your Expectations

  • 30+ Years of Experience

  • 30+ clinical trial centers across the U.S.

  • 30+ new drug approvals in the past 5 years

  • 8,000+ studies completed across all phases

  • 1M+ participants in database

  • 100+ investigators in multiple specialties

AMR Clinical’s proven approach keeps timelines on track and ensures quality without compromise. 

Patient Experience

AMR Clinical’s Patient Experience team develops and implements best practices for clinical trial recruitment and retention efforts across a broad range of therapeutic areas with the participant journey at the forefront of all efforts. 

Our Recruitment Center of Excellence, as part of our Patient Experience team, handles over 1.5 million participant engagement points per year. Through flexible scheduling and clear study expectations, we ensure a seamless participant experience, rapid enrollment, and exceptional retention.  

Technology

We leverage cutting-edge solutions like Advarra (CTMS, Study Collaboration, and eSource+), Veeva eReg (Site Vault Enterprise), ComplianceQuest (QMS), and Sage LMS (via ADP). AMR Clinical also utilizes multiple external data sources for participant-level insights. 

Rapid Startup

With central IRB relationships and dedicated startup team, we accelerate activation. Our streamlined processes deliver contract and budget turnaround in 48-hours or less. 

Participant Diversity

We prioritize diversity by fostering trust, improving accessibility, and expanding opportunities. Our enrollment strategy reflects the communities we serve with the goal of making research more inclusive. 

Operational Consistency

AMR Clinical is a fully integrated platform and employs consistent standard operating procedures across all our research centers. This allows us to start efficiently and execute studies on time and on budget, reliably delivering the results needed to bring new treatments to market. We understand the need for quality results fast and embrace the solutions to deliver them.

What Clients Say About Our Clinical Study Services

One benefit of using AMR Clinical sites that I want to mention is having a single escalation point of contact.

CRO, Project Manager

Your site worked as a cohesive team unlike any site I’ve been associated with. You met or exceeded every timeline without complaint. Your data were thorough and accurate; screen failures were minimal due to your excellent pre-screening. There is no one at your site who is not outstanding.

Clinical Monitor

Our company has interacted successfully with nearly all of the AMR Clinical sites. In fact, one of the AMR Clinical PIs contributed key knowledge that led to our suggesting re-design of a sponsor’s study. The suggestions simplified the study and impressed the sponsor so much that we won the business. I attribute this to the AMR Clinical site!

CRO, Division President

This is the most responsive and diligent group of sites I have ever seen with regard to eCRF completion and query resolution.

CRO, Data Manager Director

I thank all the AMR Clinical team for helping us to reach our goal of 200 randomized, and your site helped us do that two days earlier than planned. We also send our thanks for all your efforts in helping us meet this goal on time.

CRO, Senior Clinical Project Manager

See how we can support your trial.

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