Our coordinator training program now includes choices! Now you can choose our introductory, short course in Good Clinical Practice or utilize the blended-option of the short course plus our famous, 2-day interactive seminar, “Fear No Yellow Stickies”. Either way, you’ll find our courses will exceed your expectation in quality, practicality, and immediate-use in coordinating clinical research studies.
Course: Good Clinical Practice (GCP) for the Clinical Research Professional Our short course, Good Clinical Practice for the Clinical Research Professional program is now available as a CD-ROM or on-line. If your training goals include an introductory course which goes beyond most typical GCP training programs, we’ve got the course for you! Terminology, definitions, and some of the basic concepts “about clinical research” come packed in this online course with loads of practical advice! The online course also include direct links to FDA’s website where you can reference the Regulations. An extensive online glossary is also available and this course remains available to attendees as an ongoing, reference… and yes, the course also comes with contact hours which may be used for continuing education requirements!
As our introductory GCP course, this 4-hour course covers the following key topics:
The Drug Development Process as It Relates to the Clinical Research Professional
Ethics and Human Subject Protection
Clinical Trials versus Routine Medical Care: The Clinical Management of StudyParticipants
Course: "Fear No Yellow Stickies" Maximize your learning…participate in our on-line introductory GCP course then attend our internationally-acclaimed CRC workshop!
Join us for an incredible learning, networking, and interactive experience targeted to the new study coordinator. With this blended-learning opportunity, attendees participate in our online, GCP training course prior to attending the 2-day, interactive seminar. With time to learn terminology, definitions, and some of the basic concepts “about clinical research” via the online course, the workshop is devoted entirely to the day-day, practical aspects of coordinating a study. And even better, the online course remains available to attendees as an ongoing, reference and also comes with contact hours which may be used for continuing education requirements!
“Can’t-Miss” topics covered in the combined-program include:
Ways to ensure protocol-compliance in FDA-regulated studies
What’s important in conducting and documenting the informed consent process
What are “source documents” and how do I get this into what….oh yes, CRFs???
Why does everyone want me to describe “side effects” as “adverse events”?
Stress reduction and relaxation for clinical research professionals
Adverse events, drug accountability, what monitor’s expect, and much, much more!
Format: Blended learning program which includes both an online program plus interactive workshop. All workshops conducted in New Orleans! Click here for upcoming workshop dates.
