Clinical Trials and Medical Research Studies in Columbus Ohio

Medical Miracles come from Everyday Heroes.

614.501.6164
Columbus Clinical Research
99 North Brice Rd, Suite 260, Columbus, OH 43213

Sponsors

Columbus Clinical Research has several key strengths that enable us to provide outstanding service to our sponsors:

  • We provide outpatient services in a modern 3,000 square foot clinical research facility.
  • Columbus Clinical Research utilizes a central IRB with a 24-48 hour turnaround time for regulatory, budgets and contacts.
  • A comprehensive volunteer tracking system.
  • Experienced staff who are CPR and IATA certified.

Types of Clinical Studies we undertake

  • Birth Control
  • Hypercholesterolemia
  • Irritable Bowel Syndrome
  • Gout
  • Duodenal Ulcer & Gastric Ulcer
  • Rheumatoid Arthritis
  • Diabetes
  • Asthma
  • Obesity
  • Irritable Bowel Syndrome
  • Influenza
  • Allergic Rhinitis
  • Fibromyalgia
  • Migraine Headache

Our Clinical Research Facility includes:

  • IATA and CLIA certified
  • -80 degree freezer
  • -20 degree freezer
  • Overnight visits
  • 10 patient beds
  • 10 patient exam rooms

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Staff Credentials

Dr. Samir Arora is Board Certified in Family Medicine as well as CPI certified. He has been doing research for over ten years.

All staff are CPR and IATA certified. The experience level of our coordinators ranges from three to fifteen years, with an average of 10.

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Enrollment Capacity

We use utilize Clinical Conductor, a Clinical Trial database system that lets us track and monitor all of our patients. Our database consists of over 9,000 patients and is continuously growing. Columbus Clinical Research is known as one of the leading enrolling research facilities in Ohio. We pride ourselves in enrolling quality volunteers at a rapid rate.

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Volunteer for a Clinical Trial





Quality Assurance Department

  • Standard operating procedures annually reviewed and updated.
  • Internal auditing including tracking of error rates, query rates and interventions.
  • Patient surveys given at end of visits.
  • Monthly staff meetings to review studies and educational material.

Volunteer Demographics

  • Standard operating procedures annually reviewed and updated.
  • Internal auditing including tracking of error rates, query rates and interventions.
  • Patient surveys given at end of visits.
  • Monthly staff meetings to review studies and educational material.

IRB Central

Columbus Clinical Research utilizes a central IRB. Our turnaround time for regulatory, budgets and contacts is 24-48 hours. We do not have to have a contract signed before we can proceed with regulatory documents.