Ophthalmic Research Training - Clinical Research Training Ophthalmologist & Ophthalmology

Ophthalmic Research Training
9050 Summerfield Rd
Temperance, MI 48182

Telephone:

(419) 343-7384

Clinical Research Coordinator Intermediate Training A-Z

Ophthalmology is a branch of medicine which deals with the diseases and surgery of the visual pathways, including the eye, hairs, and areas surrounding the eye, such as the lacrimal system and eyelids. The term ophthalmologist is an eye specialist for medical and surgical problems. Since ophthalmologists perform operations on eyes, they are considered to be both a surgical and medical specialty. The word ophthalmology comes from the Greek roots ophthalmos meaning eye and logos meaning word, thought or discourse; ophthalmology literally means "the science of eyes". Ophthalmic Research Training Services provides Clinical Research Training for this medical discipline.

Ophthalmologists are medical doctors (M.D.) or Doctors of Osteopathic Medicine (D.O.) who have completed a college degree, medical school, and an additional four years of postgraduate training in ophthalmology in many countries. Many ophthalmologists also undergo additional specialized training in one of the many subspecialities. Ophthalmology was the first branch of medicine to offer board certification, now a standard practice among all specialties. Ophthalmic Research Training Services provides Clinical Research Training for this medical discipline.

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Ophthalmic Research Training Services - Clinical Research Training

This seminar is designed for Clinical Research Coordinators with more than 12 months of clinical research experience.

Study Coordinator Intermediate Training A-Z takes you beyond Study Coordinator Basic Training A-Z with in depth coverage of protocol evaluations, study budgets, developing a profitable research practice, design standard operating procedures for your site, informed consent process, marketing the clinical research practice and subject recruitment.

What You Will Learn

Upon completion of the seminar, participants will be able to:

Evaluate protocols for participation feasibility.
Outline key points that make a budget profitable.
Develop standard operating procedures for your site.
Differentiate the elements that make for a successful research practice.
Write an informed consent that is FDA regulation compliant.
Describe different mediums for marketing clinical research projects.
Identify ways of advertising and increasing subject recruitment.
Improve organization to increase productivity

Bonuses

The Study Coordinator Training Manual is part of the registration fee and will be presented to you at the time of seminar.

Length of Seminar

This seminar is a full 8-hour training session.

Location of Seminar

This seminar is held at our Training Facility in Dundee, MI.

Or, it can be held in your office or any city in the country.

Please contact us at 419-343-7384 for more information.