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Juno Research,L.L.C
Delivering High Quality Results
About Us

              Juno Research, L.L.C. is a privately owned Site
             Management Organization specialized in Phases II,
             III and IV Clinical Trials.
Copyright© -2004-2011 Juno Research, L.L.C

  Currently operating in five Clinical research which are conveniently locate in
  Houston's mayor urban areas, we provide our customers with the best quality
  study services by centralizing functions that guarantee optimum results.             

  Our research background, work experience, commitment to deliver high quality
  results and our large database of patients (which grows even larger by the day
  due to our recruitment procedures) give us  the benefit of trust that is attracting
  more and more Sponsors to work directly with us.

  Unlike other research facilities, we provide our customers with quality study
  services such as:


  •  Initial study feasibility
  •  Accelerated study startup
  •  Centralized management functions
  •  Rigorous internal quality control
  •  Experienced and dedicated Investigators an Study Coordinators


  Our main goal is to successfully expedite the approval and marketing of the
  products held on Trial.

  We work effectively with our sponsors to negotiate fair budgets and contracts
  that lead to win-win relationships. We offer top quality services to pharmaceutical,
  CRO and Biotechnology companies by centralizing management and regulatory
  functions, implementing standard operating procedures and providing accurate   
  study feasibility assessment along with accelerated startup

  Our mission is to dramatically improve the process of drug development by:

  •  Offering accelerated Study-Startup through complete study feasibility  reports,
         providing  fast and accurate feedback and by recruiting the necessary
         specialists for each clinical site

  •  Providing experienced and dedicated Investigators and  Coordinators.

  •   Establishing centralized management and regulatory functions.

  •  Using standard operating procedures throughout all our Clinical Sites.

  •  Utilizing Central Institutional Review Board.

  •   Ensuring rigorous internal quality control by regularly supervising and
          evaluating the work of coordinators and other Research Staff.

  •  Maintaining accurate application of specifications included in Clinical protocols