Seminar and Course Descriptions
Our 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 number and email.
Study Coordinator Basic Training A-Z Study Coordinator Intermediate Training A-Z Learn the pearls and set your research course for success! This Course is a must!
Course Description: 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. The course manual and other materials helpful to the study coordinator will be provided.
Upon completion of this course, participants will be able to:
Identify the Roles in the research practice Understand why GCP & ICH guidelines are important Prepare the regulatory processes Conduct binder maintenance & source documentation Understand site selection process and set-up Identify adverse events and reporting SAE's Maintain drug accountability logs Prepare for monitoring visits Apply the organizational tools provided Be able to seek out clinical trials This course is guaranteed to be filled with the latest information ophthalmic research has to offer.
Course Fee: $ 1,095 (Includes all course materials, instruction regulation manual, six months of free continued support via number and email.)
This Course is a must!
Course Description: This seminar is designed for Study 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.
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
This course is guaranteed to be filled with the latest information ophthalmic research has to offer.
Course Fee: $ 1,095 (Includes all course materials, instruction regulation manual, six months of free continued support via number and email.)
Note: All sales final upon completion of seminar
“Ms. Stader’s collection of ‘pearls’ and organizational tips has made me realize I can manage the day to day functions of clinical research in a very concise way. Implementing the ‘visuals’ from Study Coordinator Basic Training A-Z course, has allowed me more time to continue my educational journey in the world of clinical trials. Monitors have noticed the positive changes as well. I can’t wait to attend Study Coordinator Intermediate Training A-Z.”
~ Lisa S. Shreveport, LA
For more information on ways we can customize training to fit your needs, please contact us at:
419-343-7384
info@ortsedu.com 9050 Summerfield Rd. Temperance, MI 48182
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