• ERT (mystudy)
  • Finance
  • Firecrest
  • GCP
  • Gereatic
  • Healthcare
  • Healthport
  • Immunology
  • Inform
  • Infosario
  • Interalist
  • Internal Medicine
  • Intralink
  • IRB
  • iSite
  • IWRS
  • Lab connect
  • Lab Processing
  • LifeSciences
  • Medical Devices
  • Medicine
  • Medidata
  • Mytrials
  • NEH
  • Neurology
  • NeuroRx
  • Patient Recruitment
  • Protocol
  • RDC
  • Regulatory
  • Regulatory Submission
  • SIR
  • Trailmax
  • Vaccines
  • Venipucture
  • Web Oasis

Innovative Clinical Research Center, Inc.

  • Pearl IRB
  • Quorum IRB
  • Schulmans IRB
  • Sterling IRB
  • WIRB
  • Possis Medical
  • PRA International
  • Proctor & Gamble
  • Quintiles
  • Roche
  • Sanofi-Aventis
  • Schering-Plough
  • Sepracor
  • SK LifeScience
  • Solvay
  • St. Jude
  • Sun Pharm Advanced Research
  • SUN Pharmaceuticals
  • Sunovion
  • Takeda
  • The Medicines Company
  • UCB Biosciences
  • Vaccinex, Inc.
  • Wyeth
  • Forest
  • Genentech, Inc.
  • GlaxoSmithKline
  • Guidant
  • i3 Research
  • ICON
  • Inc Research
  • Janssen
  • Johnson & Johnson
  • Lilly
  • Lundbeck
  • Medtronic
  • Merck
  • Novartis
  • Opexa Therapeutics
  • Optum
  • Otsuka
  • Parexel
  • Pfizer

Innovative Clinical Research Center, Inc. prides itself on our experienced, professional team that includes: Registered Nurses, dietitians, certified medical assistants, certified clinical assessors and raters, regulatory specialist, certified clinical research coordinators and accounting assistant / IT associate. ICRC will be partnering with an array of pharmaceutical companies to perform cutting edge research specifically designed to determine the efficacy ratings of new medications before they come to market. We will be partnering with various physicians that will serve as the principal investigator on the research studies thus providing excellent care for the patient and quality data for the sponsor.  ICRC does conduct Phase I - IV clinical trials in different therapeutic areas, this is an essential component of the process of expanding knowledge and hopefully contribute to the management and cure of numerous afflictions that affect so many people today. And, because we are a dedicated clinical research site company, all of our clinical research coordinator commits 100% of their time to our research studies. Our entire medical staff is highly committed to providing exceptional care to the volunteers that participate in our clinical research studies and outstanding service to our pharmaceutical, biotech and contract research organization (CRO) clients.

Regulatory Submission Turn-Around Time: 2 Business Day(s)
Contract Turn-Around Time: 2 Business Day(s), with execution of final within 2 Week(s)


  • Onsite Lab with CLIA waiver
  • Emergency Medication
  • Defibrillator
  • Oxygen
  • BLS / AED Certified Staff
  • IATA, HIPAA & OSHA Compliant
  • Site Specific SOP’s
  • Fully Equipped Private Exam Room
  • Ambient Centrifuge
  • Adult Portable Sphygmomanometers (Electronic & Manual)
  • Digital Patient Thermometer
  • Pulse Oximeter
  • -20 Degree Freezer
  • Secure, Double-Locked IP Storage



  • IP and refrigerator Min/Max Temperature Monitoring
  • In House ECG Equipment (Atria 3100) – ability to transmit by analog line
  • Detect-o standard manual scale with height measurement (lbs)
  • Weight Gurus Bluetooth Smart Connected Body Fat Scale (lbs/kg) (Measures: weight, BMI, Body Fat, Muscle Mass, Water Weight and Bone Mass)
  • Ample Patient Waiting Area
  • Private Staff Kitchen
  • Large Conference Room
  • Within 2 miles from Hospital
  • Secured Long Term Filing Storage
  • WIFI (High Speed Internet)
  • Central IRB Capabilities
  • Comfortable Private Monitoring Space
  • Copy, Fax and Phone Accessible to Monitors
  • Dry Ice Access
  • Experience Certified Clinical Research Coordinator(s)
  • IATA Certified
  • C-SSRS Certified
  • CRCP Certified
  • CCRP Certified
  • Convenient to Charlotte Douglas International Airport
  • Close to Major Hotels and Restaurants
  • Plenty of Parking
  • Full Time Coordinator(s) trained in:

       -Good Clinical Practices (GCP)
       -Standard Operating Procedures (SOP’s)
       -Venipuncture / Injections
       -Holter Monitor


  • MAGI certified (CRCP)
  • Medidata certified
  • SOCRA certified (CCRP)

We also have a Notary on our staff (if needed)

IRB(s) we use:

  • Aspire
  • Chesapeake IRB
  • CIRB
  • Copernicus IRB
  • New England IRB

Innovative Clinical Research Center, Inc., founder, Investigator(s), Rn(s), CRC(s) and Staff members collectively have over 76 years’ experience in the medical field and 34 years in the medical research field.

Here are some of the pharmaceutical, sponsors and CRO’s we have partnered / worked with in our past years of experience (but not limited to):

  • Abbott
  • Amgen, Inc.
  • AstraZeneca
  • AtheroGenics
  • Berlex
  • Biogen Idec
  • BioRASI
  • Boehringer Ingelheim
  • Boston Scienific
  • Bristol-Myers Squibb
  • Cardiovascular Research Foundation
  • Chelsea Therapeutics
  • Chiltern
  • Chugai Pharmaceutical
  • Civitas Therapeutics, Inc
  • Cordis
  • CSL Behring
  • Daiichi Sankyo
  • EMD Serono

Skill we possess:

  • Agastha
  • Biomedical
  • Biotechnology
  • Box
  • Cardiology
  • Cardioportal
  • CFS
  • ClinCard
  • Clinical Development
  • Clinical Monitoring
  • Clinical Trial Research
  • Clinphone
  • CNS disorders
  • Contracts
  • Corelab
  • Datalabs
  • Diabetes
  • eDC
  • Egent Card

At Innovative Clinical Research Center Inc., we know that high quality research sites will always be in demand and we aim to be the best. We are committed to strictly adhering to the highest ethical standards for the care and protection of subjects in Pharmaceutical Research. 

For CRO’s and Sponsors who would like to discuss clinical trial opportunities, please contact:

Myrna Shrum
Innovative Clinical Research Center, Inc.
Tel: 704-321-4488 Ext. 1
Email:  mshrum@icresearchcenter.com

Links for Clinical Research Professionals (feel free to bookmark this site for future reference): 

http://www.fda.gov/cder/index.html - Get the latest on Drug developments from the FDA. 

http://www.accessdata.fda.gov/scripts/cder/drugsatfda - Find package inserts for and information on all approved medications. 

http://www.fda.gov/oc/gcp/regulations.html - FDA Regulations relating to Good Clinical Practice and Clinical Trials. 

http://www.fda.gov/cder/guidance/959fnl.pdf - Guidance for Industry; E6 Good Clinical Practice: Consolidated Guidance. Use this link in the event that you do not have this memorized already. 

http://www.nihtraining.com/ohsrsite/guidelines/guidelines.html - Regulations and Ethical Guidelines. The link includes the Nuremberg Code, the Belmont Report and the Declaration of Helsinki.