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Managing clinical trials for over 30 years

Remington-Davis is a Columbus-based independent research site and clinical trial management partner providing unmatched enrollment speed, expertise and flexibility for patients and sponsors. With more than 30 years of experience in the industry, we understand the challenges of clinical study management and making patients feel valued.

Our location and extensive patient database allows us to recruit diverse populations quickly, while our caring staff and home-like setting contribute to an exceptional patient experience.

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2-day

Contract Turnaround Time 
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15+

Top Physicians
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16k+

Patient Database
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35%

Patient
Diversity Rate
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24Hrs.

Response to
Patient
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3-Day

IRB Submission
Clinical trial managers, like the trial manager featured here, prioritize the patient experience while ensuring adherence to regulatory compliance protocols

An exceptional patient experience

We take pride in providing a warm, caring, and secure environment for our clinical trial patients. We have private rooms to accommodate patients overnight, and we offer flexible appointment times to work with patients’ busy schedules. Our clinic is conveniently located close to downtown Columbus, near many hotels, restaurants, and shopping centers.

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  • Simplified clinical trial site selection 

  • Faster clinical trial patient recruitment 

  • Efficient study start-up 

Simplified clinical trial site selection 

Simplified clinical trial site selection 

We know how difficult it can be to find the right combination of clinical trial sites to meet your needs. As an independent research site with 30 years of experience and over 600 completed studies, we are a trusted clinical trials management partner to have in your network.

Faster clinical trial patient recruitment 

Faster clinical trial patient recruitment 

Industry research shows nearly 80% of clinical trials fail to enroll patients in a timely manner, leading to delays. Our team understands the importance of diverse clinical trial patient enrollment, and we have the network and the partnerships to make it possible. We work with a variety of physicians and community groups to help your team meet the FDA requirements for clinical trial Diversity Plans. We also use numerous advertising outlets, full-time recruiters and a 24-hour hotline.

We’re proud to have a 35% patient diversity rate and clinical trial patient enrollment and retention rates that are significantly higher than the industry average.

Efficient study start-up 

Efficient study start-up 

Our team is committed to fast, efficient study start-up. With a turnaround time of just two days for contract execution and faster IRB submission, we set the pace for turnkey studies to help you meet the requirements of regulatory agencies and bring your drug or device to market sooner.

Comprehensive, flexible clinical trial management

Our clinical trial management services help you avoid delays while putting patients and sponsors at ease. We recognize every clinical trial is unique, and as a smaller clinical research site, we have the flexibility to accommodate changes or special requests along the way.

Two members of a research team can access up-to-date clinical trial data and study documents via a clinical trial management system

Preserving data integrity every step of the way

Clinical trial data management can be a challenge, particularly for decentralized trials. We use leading-edge technology to ensure all patient data we collect is accurate, reliable, and secure, leading to faster approvals. 

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Professional clinical research staffing expertise at every level


Our clinical research staffing model provides each study with a trusted physician and experienced team members, ensuring our studies are conducted with the highest standards of professionalism and expertise. Our physicians have expertise in over 20 therapeutic areas, including:

  • Internal medicine
  • Pulmonology
  • Dermatology
  • Endocrinology
  • Infectious disease
  • Immunology
  • Nephrology
  • Gastroenterology
Meet our Physicians
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Every breakthrough has a beginning. Start yours.

At Remington-Davis clinical research, we are committed to advancing healthcare through our dedicated efforts in clinical trial management. Whether you're a sponsor, CRO, research associate, patient or healthy volunteer, we invite you to join us on the journey towards medical breakthroughs. 

Schedule a 30-minute consultation with us to discuss your patient recruitment and
enrollment challenges and learn how we can help with your clinical trial management.

Schedule a Consultation