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Research Center Profile:
Remington-Davis Clinical Research

Center Information

Hamish Baird, MBA
Director of Business Development
Remington-Davis Clinical Research
1335 Dublin Rd, Suite 106A
Columbus, OH 43215
USA
614-487-2560
614-486-4123 (fax)
info@remdavis.com
www.remdavis.com
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Contact Center

Therapeutic Areas

Cardiology/Vascular Diseases
Devices
Endocrinology
Gastroenterology
Hematology
Immunology
Infections and Infectious Diseases
Internal Medicine
Musculoskeletal
Nephrology
Neurology
Ophthalmology
Orthopedics/Orthopedic Surgery
Pharmacology/Toxicology
Pulmonary/Respiratory Diseases
Rheumatology
Trauma (Emergency, Injury, Surgery)

Center Overview

Remington-Davis, Inc. Clinical Research was founded in 1992 to assist local physicians conduct phase I-IV pharmaceutical industry sponsored clinical trials within their own private practice or hospital setting. Remington-Davis has developed into a multi-specialty investigative research center coordinating all aspects of research trials including investigator recruitment, IRB correspondence, contracts & budgets, protocol development, patient enrollment, data collection and regulatory compliance.

Remington-Davis has trial experience in 18 therapeutic areas and relationships with 3 area hospitals and 10 clinics and physicians’ offices. Through our contacts and experience, we provide our pharmaceutical sponsors and contract research organizations with access to the top investigators and a database of over 10,000 patients in the central Ohio area.

Why we are Different:

  • Research is our ONLY business
  • In-patient and Out-patient capabilities and experience
  • Full-time Dedicated Regulatory Personnel
  • Experienced Coordinators focus on finding and enrolling evaluable patients
  • Top Investigators participate in our studies because of our high quality and success, not exclusive contracts

Vision Statement:

We provide a link between the community of today and the health care of tomorrow

We are committed to our values both individually and as a team:

  • Providing scientific information that will improve healthcare for the future
  • Earning respect and trust through ethics and honesty

Performance Metrics

Number of Studies Conducted: 522
Number of Studies Actually Completed: 503
Number of Active Patients in the Database: 50000
Regulatory Submission Turn-Around Time: 5 Business Day(s)
Average Number of Total Patients Enrolled: 10
Average Percent of Total Patients Randomized: 75%
Average Percent of ‘Completed’ Studies that met Enrollment Goals: 93%
EDC Capabilities: Yes

Clinical Research Experience

Our Excellence is evidenced by repeat business with major pharmaceutical sponsors, over 325 studies conducted in 18 therapeutic areas and enrollment of thousands of evaluable patients.

We have worked with the following sponsors and CROs:

  • Abbott Laboratories
  • Adolor
  • Alpha Therapeutic Corporation
  • APEX-Bioscience
  • Aronex Pharmaceuticals
  • Astra Merck
  • Aventis
  • Bayer Corporation
  • Boehringer Ingelheim Pharmaceuticals, Inc.
  • Bristol-Myers Squibb Company
  • Cambridge NeuroScience, Inc.
  • CATO Research
  • Centeon
  • Centocor Pharmaceuticals
  • Chiron
  • ClinTrials Research
  • Coagulation Diagnostics
  • Concepts in Pharmaceutical Research (CPR)
  • Covance
  • CroMedica Inc.
  • Cubist
  • Dey Laboratories
  • Discovery Laboratories
  • Dupont Pharmaceuticals
  • Eisai
  • Eli Lilly
  • Fact Flow Research
  • Forest Research Institute
  • Genomics
  • Gilead
  • Glaxo Wellcome
  • Icon
  • Immunex Corporation
  • Janssen Research Foundation
  • Johnson & Johnson Pharmaceuticals
  • Kendle
  • Knoll Pharmaceutical Company
  • Lipsome Company, Inc.
  • Merck & Company
  • Novartis
  • Ohmeda Pharmaceutical Products
  • Omnicare
  • Organon
  • Ortho-McNeil Pharmaceuticals
  • Parexel
  • Parke-Davis Pharmaceuticals
  • Pfizer
  • Pharmaceutical Research Association
  • Pharmacia & Upjohn
  • PharmaResearch Corporation
  • PPD, Inc.
  • Quintiles, Inc.
  • Reliant
  • Roerig-Pfizer Pharmaceuticals
  • Roxane Laboratories
  • Sanofi
  • Schering Plough
  • Scirex
  • SmithKline Beecham Pharmaceuticals
  • Spectrum Pharmaceutical Research Corporation
  • SYNSORB
  • Takeda
  • ViroPharma
  • Wyeth-Ayerst
  • Yamanouchi

Facility Description

Remington-Davis is located in a convenient location close to downtown Columbus, Ohio and is approximately 15 minutes from the Columbus International Airport. In addition to on-site clinical facilities, Remington-Davis has immediate access to the following:

  • Three Major Medical Centers
  • Level 1 Trauma Center
  • Outpatient Surgical Center
  • Endoscopy Center
  • 24-hour staffing and study visit capability
  • Late Phase I Study experience
  • Pharmacy
  • Microbiology Laboratory
  • Clinical Laboratory
  • Radiology Laboratory
  • Centrifuge
  • Refrigerated Centrifuge
  • Freezer (-20 to -8&degC)
  • Freezer (-70&degC)
  • Secure Drug Storage
  • Secure Record Retention

Investigator Experience

Remington-Davis, Inc. has existing relationships with over 30 of the best physicians in the central-Ohio region representing over 18 therapeutic areas:

  • Cardiology
  • Critical Care
  • Device
  • Emergency Services
  • Family Practice
  • Gastroenterology
  • Infectious Diseases
  • Internal Medicine
  • Neurology
  • Neurosurgery
  • Oncology
  • Orthopedics
  • Pulmonary Medicine
  • Radiology
  • Surgical Oncology
  • Trauma

Our Investigators are not bound by contract - they continue to participate in studies with us because of our excellent results and successful working relationships.

Staff Expertise

The management team at Remington-Davis has 39 collective years of dedicated clinical research experience.

Hamish Baird, MBA
Vice President and Business Development

Jennifer Botte, RN, CCRC
Director of Inpatient Services

Laura Cooper, BS
Director of Outpatient Services

Rebecca Baird, RN, CCRC
Director of Research

Haley Bakies, BA
Regulatory Coordinator

Dedicated Regulatory Staff

  • We boast full-time regulatory employees
  • Our dedication to regulatory accuracy results in fewer monitor queries, faster turnaround times, and better results
Coordinators
  • We have 9 full-time coordinators who manage no more than four studies at any given time
  • Our coordinators have science and medical backgrounds, hospital privileges, and a passion for research

Other Information

Our Services:

  • Dedicated, in-house coordinators ENROLL
  • Full time regulatory team ENSURES QUALITY DATA
  • Knowledgeable and friendly support staff make COMMUNICATION EASY
  • Top Investigators CONCENTRATE ON MEDICAL MANAGEMENT because we do the recruiting and administrative work

Other capabilities include:

  • Centralized Contracting and Budgeting
  • Centralized Regulatory Data Collection
  • Central IRB Approval
  • Remote Data Entry
  • Protocol Writing
  • Regulatory Consulting
  • Coordinator Training
  • Investigator Recruiting and Training
  • Advertising for Patient Recruitment

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.

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