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Phoenix Clinical Research was established in 2006 and is housed in a modern 10,000 square foot facility under the supervision of board-certified orthopedic surgeon, Dr. Richard Berkowitz.

Dr. Berkowitz has been in private practice since 1996 and has participated in clinical research trials as both a Sub-Investigator and a Principal Investigator. He is a member of the Society of Clinical Research Associates (SOCRA) and is a Certified Clinical Research Associate. Dr. Berkowitz supervises his staff in conducting a variety of medical studies, including Phase II , III, IV and V clinical trials as well as orthopedic device studies.

The strong relationship Dr. Berkowitz has with his patients facilitates patient enrollment in studies and is associated with a low drop-out rate once studies have begun. Phoenix staff members provide study sponsors with the same kind of personalized attention that is provided to their patients and assures sponsors that their study protocols are well-managed and successfully executed. We offer sponsors a quality research environment with a trained and experienced research staff that adheres to the highest ethical, regulatory, and industry standards. Our staff members are regularly involved in continuing education programs to stay current on industry standards.


Demographic Data

  • Start year clinical research2005
  • Phases of clinical studiesPhase II, Phase III, Phase IV
  • Types of studiesBiologics, Drugs, Medical Devices
  • # of employees involved in research4
  • Days openMonday, Tuesday, Wednesday, Thursday, Friday
  • Extended office hoursYes
  • Overnight facilitiesYes
  • Dry iceYes
  • Blinded pharmacistYes
  • Dedicated monitoring spaceYes
  • Internet access for the monitorYes
  • Onsite laboratoryYes
  • Central laboratoryYes
  • Shipping optionsFedEx, UPS, DHL
  • Contact for regulatory documentsSteffanie Littleton
  • Regulatory phone number754-205-5000
  • # of days to turn around regulatory documents5
  • Type of IRB used by this siteCentral
  • Appropriate storage facilities for productYes
  • Able to appropriately store Schedule II drugsYes