Ophthalmic Research Training
9050 Summerfield Rd
Temperance, MI 48182
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(419) 343-7384 |
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Clinical Research Associates (CRAs) - Monitors
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As a monitor you are the eyes and ears of the Sponsor/CRO.
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| FACT: |
It's difficult to be meticulous if you don't understand the records you're reviewing.
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| FACT: |
You can't be an effective leader when the site understands more about ophthalmology than you do.
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As a Clinical Research Associate (CRA) you are taking complete responsibility for site management of the
clinical research data collection and validation process, AE reporting and confirmation the site is following
required regulatory procedures. But...
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Do you have a solid understanding of ophthalmic 'lingo' and acronyms?
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Do you understand the various charting differences especially if monitoring a retina study?
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Do you find you are less productive during your site visits due to poor preparation from the site?
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Do you find yourself wasting valuable time continually going over the basics with the study coordinator?
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Do you find that the action items listed in your monitor letter have been repeatedly unaddressed by the site?
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Are you looking for templates that will help make your day-to-day monitoring duties easier?
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Do your fellow Clinical Research Associates (CRAs) experience the same situations?
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Ophthalmic Research Training Services comprehends these situations and provides the training, tools and support
required to be highly successful in your research career.
Get started on the right Ophthalmic Research Training plan today. It's so easy, just email or call me for a free confidential consultation
of your research needs.
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