Sponsors and CROs
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Ophthalmic Research Training Services, LLC has earned the trust and respect of the research field due to our ability to listen to the needs of the individual research Sponsors and Contract Research Organizations and develop solutions to meet their goals.
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Do you currently have ophthalmic protocols in place or are looking at new ophthalmic protocols or pilot studies in the future?
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Do you have CRA’s with ophthalmic experience?
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Are your current CRA’s frustrated due to a need for ophthalmic training?
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Do you want your CRA’s to be able to validate accurate information for your organization due to their abilities to navigate in ophthalmic source documents and charts with ease?
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Do you want your CRA’s to appear educated and confident with ophthalmic terminology to the sites coordinators and PI’s?
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Do new sites for these protocols have well trained clinical research coordinators in place?
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Do you have the team and the time to bring these new sites up to speed in clinical research thereby ensuring clean data collection and timely recruitment?
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Ophthalmic Research Training Services Can Help!
Ophthalmic Research Training Services can provide help for varying situations. "ORTS" can customize training to fit your specific needs.
Study coordinator training that can be included in conjunction with your start-up meeting so everyone is on the same level. Or training can be provided for site-specific situations at a separate time.
Other services we provide include:
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Extensive ophthalmic training for your CRA’s in record review, terminology and ophthalmic anatomy.
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‘Struggling’ site training, to help those that are in emergent need
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Protocol development aid
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CRF development aid
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Pre-Study visits
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Site qualification visits
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Regulation document collection
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Shadow CRA’s to enable them to learn in a hands-on setting.
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Now is the time to for you to take control, get an edge on improving recruitment and retention at your sites by having well trained study coordinators and CRA’s in place.
Ophthalmic Research Training Services (ORTS) understands that 90% of all protocols fail to recruit in the allowed timeframe. We understand the billions of dollars lost in delays. Shifting the focus of comprehensive training to the front end of the trial is beneficial in that, projects will launch in a timely manner, GCP, ICH and FDA regulation training doesn’t fall onto the monitor’s shoulders.
It’s a fact; well-trained confident sites continually display higher recruitment performances.
Our training services, offers a series of teleclasses specifically aimed at training the sites to be more effective at subject recruitment and retention.
These teleclasses can be incorporated into your own training program or offered to your sites that are failing to meet the anticipated recruitment goals.
Training services provided include:
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In office training – We can train the entire staff at once in their own office setting with hands-on expertise. Our professional trainer will go to their office, educate and prepare the staff to organize their research regulatory documents, learn the value of subject recruitment and retention, and display the ability to perform as a knowledgeable research team.
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Seminars – Full day seminars conducted at our training facility in Novi, MI,
Study Coordinator Basic Training A-Z - designed for coordinators with little or no research experience. Study Coordinator Intermediate Training A-Z – designed for Coordinators with more than 12 months research experience.
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Teleclass Series – An ongoing series of teleclasses that allows the study coordinator to receive training without leaving the office. Each series is aimed at areas of specific needs as requested by study coordinators and physicians. Listings on our calendar.
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6 Months Free Continued Support – No other company offers this service for personnel training! Call or Email us with your questions or concerns.
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Regulation Binder Training Manuals – Included in all training service. Provides the study coordinator with the information on how to set up and maintain ‘Reg Binders’ as well as a glossary and FDA guidance material. Organizational pearls and tools that can be utilized to aid in the day to day functions performed by study coordinators.
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Ophthalmic Research Training Services, LLC has earned the trust and respect of the research field due to our ability to listen to the needs of the individual research Sponsors and Contract Research Organizations and develop solutions to meet their goals.
Furthering educational levels of knowledge of CRA’s and study coordinators by continuing to offer training at the basic and intermediate levels.
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Allow Ophthalmic Research Training Services to come into your office, educate your staff, organize your research regulatory documents and set a course for success!
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