Ophthalmic Research Training - Clinical Research Training Ophthalmologist & Ophthalmology

Ophthalmic Research Training
9050 Summerfield Rd
Temperance, MI 48182

Telephone:

(419) 343-7384

Clinical Research Coordinator Basic 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 is a comprehensive introduction to Clinical Research for Allied Health Personnel. The foundational preparation required for the role of Clinical Research Coordinator will be provided in a practical unison of the "how-to's and why's" which is information that will successfully address the specific tasks you perform as a Study Coordinator.

Seminar attendees receive the valuable training and tools needed for excellence in job performance along with 6 months of continued support with our consultants via the toll free number and email.

What You Will Learn

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

Identify the Roles in the research practice, PI, CRC etc.
Understand why GCP & ICH guidelines are important.
Prepare the regulatory processes.
Conduct binder maintenance & source documentation.
Understand site selection process and set-up.
Proper Informed Consent Process.
IRB Submissions and approval tracking.
Identify adverse events and reporting SAE's.
Maintain drug accountability logs.
Prepare for monitoring visits.
Apply the organizational tools provided.

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.