Overview

North Carolina Clinical Research (NCCR) is an independent, multi-therapeutic outpatient clinical research site located in Raleigh, North Carolina. NCCR has conducted Phase I, II, III and IV clinical trials in both children and adults since 1986. We have completed over 693 studies in a variety of therapeutic areas for many different pharmaceutical companies and Clinical Research Organizations (CROs). The NCCR facilities and staff are dedicated 100% to Clinical Research.

We believe it is our dedicated staff at NCCR that makes our facility stand out above the rest. Our hardworking, passionate, friendly crew makes studies placed at NCCR a positive experience for both the sponsor and the patient.

Advantages we offer at NCCR:

• Consistently meet or exceed enrollment expectations
• Excellent patient compliance and retention record
• Flexible scheduling for patients
• Timely turnaround of regulatory documents and contracts
• Utilize both central and local IRBs
• Standard Operating Procedures in place
• Emphasis on the use of Good Clinical Practices to meet each sponsor’s needs
• Easy access to Investigators
• Access to a metropolitan population exceeding 1 million, including 3 major universities
• Research database of over 2700 patients

Experience

NCCR has been involved in clinical research since 1986. We focus on phase I, II, III, and IV research. We have conducted research in the following areas:

We have worked previously with the following Sponsors and CROs:

Facility

NCCR’s facilities include the following:

• Located across the street from a major medical center
• Individual monitor areas convenient to telephone, fax, copier and high speed Internet (fiber)
• Secured storage for ambient and refrigerated study drug
• Conference room
• Fully equipped lab
  • -70° C freezer
  • -20° C freezer
  • refrigerated centrifuge
  • Purifier biological safety cabinet (clean hood)
  • backup generator
  • Sensaphone temperature monitoring system
• Convenient X-ray facility
• Examination rooms (8)
• Spirometry and methacholine challenge rooms
• Treadmill (exercise challenges)
• ECG capabilities
• Easy accessibility to physicians
• Patient lounge area for extended days
• Infusion and PK capabilities
• Overnight facilities with showers and individual sleep areas
• Pollen reporting
• Internet (VOIP fiber network and wireless) capabilities

Staff

Supporting our principal investigators in the completion of each study is a clinical research staff of more than 8 professionals including Sub-Investigators, Site Manager, Subject Recruiter, Regulatory Administrator, Clinical Research Coordinators, and Office Coordinator. Our team has over 215 combined years of Clinical Research experience.

Dr. Craig LaForce is the Medical Director of North Carolina Clinical Research.Dr. LaForce has served as the Principal Investigator for approximately 560 studies and a Sub-Investigator for a handful of trials as well. Dr. LaForce is Board Certified in Allergy/Immunology and Pediatrics. He is also a Certified Physician Investigator (CPI) and is a "hands on" Investigator (Click here for more information).

Dr. Karen Dunn is the Assistant Medical Director at NCCR and has served as either the PI or Sub-Investigator since 1988. Dr. Dunn is Board Certified in Allergy/ Immunology and Pediatrics and is also a Certified Physician Investigator (CPI).

Patti Becherer has been the Clinical Research Manager at NCCR since 1989. She has a B.S. in Nursing and is a Certified Clinical Research Coordinator (CCRC). Ms. Becherer has been involved in Clinical Research since 1986. As Site Manager she is responsible for overseeing all aspects of clinical trials at NCCR.

Our Clinical Research Coordinators (CRC) are the key to the success of a study. The CRCs are responsible for the day-to-day progress of each study. Our CRCs are all trained professionals with a variety of medical and research backgrounds, including RNs, LPNs, Medical Assistants, EMT, Paramedics, CCRCs, etc. Together our 4 coordinators have an average of 20 years of experience in Clinical Research. Their qualifications include but are not limited to:

• Biennial GCP Training
• CPR Certified
• OSHA Compliant
• IATA Certified
• Experienced with several EDC, IVRS and E-Diary systems
• Trained in ECG procedures, Phlebotomy, Spirometry, FENO Testing, Allergy Skin Testing, Methacholine challenge, Exercise challenge

Jan Pochis has served as our Regulatory Administrator since 1997. Jan is CCRP (Certified Clinical Research Professional) and is responsible for all aspects of the regulatory filing and reporting in connection with our studies. Jan communicates with the IRBs and sponsors to assist in a smooth and timely turnaround of all regulatory documents.