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Corona
Research offers several professional services
at both our Investigative Site and Research Facility.
Investigative Site – William
F. Davitt, III, MD is the Principal Investigator for the
Corona Research Ophthalmology Study Site located at 8815
Dyer, Suite 165 in Northeast El Paso. Susan L. Parks,
MD is the Sub-Investigator for this site. Alberto (Al)
Molinar leads the team of experienced Study Coordinators and
Ophthalmic Technicians.
This Investigative Site offers:
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Phase 2-4 study conduct |
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Rapid patient enrollment |
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Block/group patient enrollment |
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In-house quality assurance review by an experienced staff |
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Monitor/Coordinator prior to review by the Sponsor’s CRA |
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Dedicated Coordinator and Research team for each trial |
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Board Certified Principal and Sub Investigators |
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Modern clinic with state-of-the-art equipment |
El Paso, Texas offers:
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A growing population in excess of 700,000 |
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A large demographically diverse population including
Hispanics, Native Americans, African Americans, and Asians |
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A high incidence of Diabetic Retinopathy, Untreated
Glaucoma, Pterygium, and Dry Eye Syndrome |
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A high incidence of Seasonal Allergies |
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An International Airport serviced by most major airlines |
Corona Research offers:
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Monitoring Services – Alberto (Al) Molinar is the Principal CRA for
Corona Research. Al has monitored and coordinated over 40 ophthalmic studies in the past 7 years. Our monitors are available to meet your monitoring needs for short or long-term projects.
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Monitor Training -
Corona Research offers ophthalmic technical training to the industry’s Clinical Research Associates. Our experienced monitors and coordinators will familiarize your research personnel with all aspects of an ophthalmology clinical trial. Your research personnel will be familiar with ophthalmic terminology, common ophthalmic medications, ETDRS Visual Acuity, Visual Fields and Visual Field results, and other ophthalmic
tests and procedures.
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Study Coordinator Training -
Corona Research offers
Clinical Trial training to the industry’s study coordinators and/or Investigators. Our experienced monitors and coordinators will familiarize your Study Coordinator with all aspects of a clinical trial. Your research Personnel will be familiar with preparing Regulatory Documents, the importance of a Study Source Document, Case Report Forms, Clinical Study Protocols, Good Clinical Practice, FDA Audits, and meeting the goals of the Sponsor. Patient recruitment instruction is also available. This training can be conducted at your site or ours. |
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