New Revenue Stream, Improved Patient Care and Participation in Research
Are you considering
incorporating clinical research into your practice? Doing clinical
research studies may provide you and your staff with intellectual
stimulation, give you the satisfaction of advancing the field of
medicine, and possibly provide new treatments for your patients. Done
well, clinical research can also generate a revenue stream for the
practice. But, how do you start?
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AC1289
Breaking into Clinical Research: Ethical, Practical and Financial Considerations
US $237.00
In this 90-minute audio conference you will learn the following:
Working knowledge of good clinical
practice (GCP) and regulations regarding human subject protection. Key
to good practice is implementing training and education into your
research practice.
Understand the differences between clinical practice and clinical research.
Bringing clinical research to your
practice is a big commitment. Tips on getting buy-in from all your
staff members so they don’t view their added duties as an imposition.
Who will lead your team as
principal investigator? Guidance on “reading” your interested
physicians and garnering their support as sub-investigators.
Understand the practical aspects
of conducting clinical trials…how to decide which trials best fit your
site’s resources and patient population…and how to evaluate protocols
for feasibility.
How to develop a marketing plan to recruit patients. Without patients/subjects to populate the study, there would be no study.
Guard against ill-prepared sites which incur all start-up costs and not realize the full potential if enrollment falls short.
Our Expert Speaker: Christine K. Pierre, RN, President and CEO, RX Trials, Inc.
Christine
Pierre is founder and president of RX Trials, Inc., an elite network of
independent in-patient and out-patient clinical research sites
strategically located throughout Maryland, Washington, D.C., and
Virginia. Ms. Pierre has spent nearly 20 years as a clinical research
professional. She has been the co-principal investigator of a
multi-center clinical trial and various single-center trials, and
co-authored many of the resulting articles. She frequently lectures,
moderates panels, and conducts workshops at national industry
conferences, and she is on the Editorial Board of Clinical Trials
Advisor and Clinical Researcher.
